SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system (Q24304950)

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English	SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system	scientific article

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instance of

scholarly article

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title

SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system (English)

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main subject

brain

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disability

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Sine oculis binding protein homolog

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stated in

GOA release 2020-03-11

cognition

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stated in

GOA release 2020-03-11

intellectual disability

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based on heuristic

inferred from title

disability affecting intellectual abilities

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based on heuristic

inferred from title

non-syndromic intellectual disability

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based on heuristic

inferred from title

author

Lina Basel-Vanagaite

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22

object named as

Lina Basel-Vanagaite

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Metsada Pasmanik-Chor

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4

object named as

Metsada Pasmanik-Chor

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David J. Tischfield

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David J Tischfield

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13

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M. Chiara Manzini

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Chiara M Manzini

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3

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Laurence Colleaux

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Laurence Colleaux

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10

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Christopher A. Walsh

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6

object named as

Christopher A Walsh

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Gidi Rechavi

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18

object named as

Gideon Rechavi

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Amos J Simon

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9

object named as

Amos J Simon

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Mordechai Shohat

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21

object named as

Mordechai Shohat

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Nurit Magal

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15

object named as

Nurit Magal

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Idit Maya

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16

object named as

Idit Maya

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Adi Har-Zahav

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2

object named as

Adi Har-Zahav

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Efrat Birk

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1

object named as

Efrat Birk

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author name string

Liora Kornreich

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5

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Konrad Noben-Trauth

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7

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Adi Albin

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8

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Yair Morad

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11

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Limor Rainshtein

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12

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Peter Wang

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14

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Noa Shoshani

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17

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Doron Gothelf

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19

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Gal Maydan

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20

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language of work or name

English

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publication date

12 November 2010

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published in

American Journal of Human Genetics

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volume

87

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issue

5

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page(s)

694-700

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cites work

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Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation

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Combination of linkage mapping and microarray-expression analysis identifies NF-kappaB signaling defect as a cause of autosomal-recessive mental retardation

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Identifiers

DOI

10.1016/J.AJHG.2010.10.005

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

835274

OpenCitations bibliographic resource ID

835274

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

835274

PMC publication ID

2978971

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

835274

PubMed publication ID

21035105

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

835274

ResearchGate publication ID

47633826

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