Voltage-gated calcium channel gamma 2 subunit gene is not deleted in velo-cardio-facial syndrome (Q74156529)

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9 November 2019

title

Voltage-gated calcium channel gamma 2 subunit gene is not deleted in velo-cardio-facial syndrome (English)

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9 November 2019

Black JL 3rd

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9 November 2019

Krahn LE

series ordinal

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9 November 2019

Jalal SM

series ordinal

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9 November 2019

publication date

1 July 2001

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9 November 2019

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9 November 2019

volume

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9 November 2019

issue

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9 November 2019

page(s)

461-464

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Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia

9 November 2019

cites work

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MRI anatomy of schizophrenia.

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Identification and cloning of putative human neuronal voltage-gated calcium channel gamma-2 and gamma-3 subunits: neurologic implications

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A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

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7 January 2021

A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12

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7 January 2021

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

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7 January 2021

Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3

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7 January 2021

Three new mutations in patients with myophosphorylase deficiency (McArdle disease)

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7 January 2021

Search for schizophrenia susceptibility genes

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7 January 2021

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

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7 January 2021

The DNA sequence of human chromosome 22

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7 January 2021

Childhood-onset schizophrenia associated with parkinsonism in a patient with a microdeletion of chromosome 22.

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7 January 2021

A common molecular basis for rearrangement disorders on chromosome 22q11

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7 January 2021

Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation.

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7 January 2021

Molecular and functional diversity of voltage-gated calcium channels

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7 January 2021

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

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7 January 2021

Functional roles of gamma2, gamma3 and gamma4, three new Ca2+ channel subunits, in P/Q-type Ca2+ channel expressed in Xenopus oocytes

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7 January 2021

Voltage-dependent calcium channel mutations in neurological disease.

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7 January 2021

Selective failure of brain-derived neurotrophic factor mRNA expression in the cerebellum of stargazer, a mutant mouse with ataxia

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7 January 2021

Cerebellar brain-derived neurotrophic factor-TrkB defect associated with impairment of eyeblink conditioning in Stargazer mutant mice.

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7 January 2021

Impaired cerebellar synapse maturation in waggler, a mutant mouse with a disrupted neuronal calcium channel gamma subunit

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7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4000868

1 reference

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9 November 2019

1 reference

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