Congenital Muscular Dystrophy Associated With Merosin Deficiency

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The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review Cell-matrix interactions in muscle disease.Genetic modelling of muscular dystrophies.

P2860

Q24680748-08D72317-E3DD-482F-B208-FC1D1F09E7FE Q37944530-AF054B0F-5BC2-4083-8853-73E976C2394F Q47950276-F245A038-8E5D-4433-80B2-89CA40D0175A

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Congenital Muscular Dystrophy Associated With Merosin Deficiency

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http://www.wikidata.org/entity/Q57394328

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im Juli 1996 veröffentlichter wissenschaftlicher Artikel

@de

scientific article published on 01 July 1996

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в липні 1996

@uk

name

Congenital Muscular Dystrophy Associated With Merosin Deficiency

@en

Congenital Muscular Dystrophy Associated With Merosin Deficiency

@nl

type

Item

label

Congenital Muscular Dystrophy Associated With Merosin Deficiency

@en

Congenital Muscular Dystrophy Associated With Merosin Deficiency

@nl

prefLabel

Congenital Muscular Dystrophy Associated With Merosin Deficiency

@en

Congenital Muscular Dystrophy Associated With Merosin Deficiency

@nl

P1476

Congenital muscular dystrophy associated with merosin deficiency

@en

P2093

A H Beggs

http://www.w3.org/2001/XMLSchema#string

F Shapiro

http://www.w3.org/2001/XMLSchema#string

L A Specht

http://www.w3.org/2001/XMLSchema#string

R K Sethi

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

The childhood muscular dystrophies: diseases sharing a common pathogenesis of membrane instability.

Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies.

A specific sequence of the laminin alpha 2 chain critical for the initiation of heterotrimer assembly.

Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons.

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

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291-295

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1177/088307389601100406

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Kathryn North

P577

1996-07-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

8807418

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Congenital Muscular Dystrophy Associated With Merosin Deficiency

about

P2860

P2860

Congenital Muscular Dystrophy Associated With Merosin Deficiency

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698