(Q48338116)

10 February 2018

title

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

1 reference

10 February 2018

author name string

Nicoline Løkken

1

1 reference

10 February 2018

Alfred Peter Born

2

1 reference

10 February 2018

Morten Duno

3

1 reference

10 February 2018

John Vissing

4

1 reference

10 February 2018

publication date

5 February 2015

1 reference

10 February 2018

published in

Muscle and Nerve

1 reference

10 February 2018

volume

52

1 reference

10 February 2018

issue

4

1 reference

10 February 2018

page(s)

547-553

1 reference

10 February 2018

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

cites work

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Clinical and pathological heterogeneity in late-onset partial merosin deficiency.

21 January 2018

1 reference

Role of laminin terminal globular domains in basement membrane assembly

21 January 2018

1 reference

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

21 January 2018

1 reference

The ever-expanding spectrum of congenital muscular dystrophies

21 January 2018

1 reference

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

1 reference

Multiplex Western blotting system for the analysis of muscular dystrophy proteins

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

21 January 2018

Identifiers

DOI

10.1002/MUS.24588

1 reference

10 February 2018

1 reference

10 February 2018