(Q58108925)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12609502%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

title

Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12609502%20AND%20SRC:MED&resulttype=core&format=json

genotype-phenotype correlation

31 October 2019

main subject

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1 reference

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6

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31 October 2019

author name string

L T Guo

1

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31 October 2019

X U Zhang

2

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31 October 2019

W Kuang

3

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31 October 2019

H Xu

4

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31 October 2019

L A Liu

5

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31 October 2019

Y Miyagoe-Suzuki

7

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31 October 2019

S Takeda

8

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31 October 2019

M A Ruegg

9

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31 October 2019

U M Wewer

10

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31 October 2019

E Engvall

11

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31 October 2019

publication date

1 March 2003

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31 October 2019

published in

Neuromuscular Disorders

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31 October 2019

volume

13

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31 October 2019

page(s)

207-215

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31 October 2019

issue

3

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Congenital muscular dystrophies: 1997 update

31 October 2019

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The ABC's of limb-girdle muscular dystrophy: alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more

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Merosin and congenital muscular dystrophy

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Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain

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Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

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PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy

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Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.

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A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy

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Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy

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Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophy.

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Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping

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7 January 2021

Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study

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7 January 2021

The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review

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7 January 2021

Animal models for muscular dystrophy: valuable tools for the development of therapies

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7 January 2021

Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats

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7 January 2021

Dystrophia Muscularis: A HEREDITARY PRIMARY MYOPATHY IN THE HOUSE MOUSE.

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Muscular dystrophy in the mouse caused by an allele at the dy-locus.

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7 January 2021

Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse

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7 January 2021

Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene

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7 January 2021

Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice

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7 January 2021

Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene

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7 January 2021

Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.

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7 January 2021

Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models

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7 January 2021

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

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy

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Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12609502%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference