(Q57990899)

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Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B

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Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B (English)

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muscular dystrophy

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Elisabeth Vafiadaki

object named as

Elizabeth Vafiadaki

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André Reis

18

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Hans Lassmann

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author name string

Reginald E. Bittner

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Louise V.B. Anderson

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Elke Burkhardt

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Rumaisa Bashir

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Silva Ivanova

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Thomas Raffelsberger

7

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Isabel Maerk

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Harald Höger

9

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Martin Jung

10

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Mohsen Karbasiyan

11

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Maria Storch

12

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Jennifer A. Moss

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Keith Davison

15

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Ruth Harrison

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Kate M.D. Bushby

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publication date

October 1999

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Nature Genetics

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23

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2

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141-142

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A comparison of muscle precursor replication in crush-injured skeletal muscle of Swiss and BALBc mice

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https://api.crossref.org/works/10.1038%2F13770

7 January 2021

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Spontaneous myopathy in the SJL/J mouse: pathology and strength loss

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https://api.crossref.org/works/10.1038%2F13770

7 January 2021

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A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p

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https://api.crossref.org/works/10.1038%2F13770

7 January 2021

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Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

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https://api.crossref.org/works/10.1038%2F13770

7 January 2021

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

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https://api.crossref.org/works/10.1038%2F13770

7 January 2021

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A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

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https://api.crossref.org/works/10.1038%2F13770

7 January 2021

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Dysferlin is a plasma membrane protein and is expressed early in human development

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https://api.crossref.org/works/10.1038%2F13770

7 January 2021

based on heuristic

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Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)

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https://api.crossref.org/works/10.1038%2F13770

7 January 2021

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A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

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https://api.crossref.org/works/10.1038%2F13770

7 January 2021

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