LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies (Q48338116)

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title

LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies (English)

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author name string

Nicoline Løkken

1

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Alfred Peter Born

2

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Morten Duno

3

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John Vissing

4

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publication date

5 February 2015

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published in

Muscle and Nerve

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volume

52

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issue

4

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page(s)

547-553

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High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency

cites work

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

21 January 2018

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Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations

21 January 2018

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

21 January 2018

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Clinical and pathological heterogeneity in late-onset partial merosin deficiency

21 January 2018

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Role of laminin terminal globular domains in basement membrane assembly

21 January 2018

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Bridging structure with function: structural, regulatory, and developmental role of laminins

21 January 2018

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The ever-expanding spectrum of congenital muscular dystrophies

21 January 2018

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Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panel

21 January 2018

1 reference

Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2.

21 January 2018

1 reference

Limb girdle muscular dystrophy due to LAMA2 mutations: diagnostic difficulties due to associated peripheral neuropathy

21 January 2018

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Multiplex Western blotting system for the analysis of muscular dystrophy proteins

21 January 2018

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Merosin-negative congenital muscular dystrophy: diffusion-weighted imaging findings of brain

21 January 2018

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Congenital muscular dystrophy with merosin deficiency: 1H MR spectroscopy and diffusion-weighted MR imaging

21 January 2018

1 reference

Congenital muscular dystrophies

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/MUS.24588

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