4.4 Article

Nemaline myopathy caused by TNNT1 mutations in a Dutch pedigree

Related references

Note: Only part of the references are listed.
Review Clinical Neurology

Congenital Myopathies: An Update

Jessica R. Nance et al.

CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2012)

Review Clinical Neurology

Nemaline Myopathies

Carina Wallgren-Pettersson et al.

SEMINARS IN PEDIATRIC NEUROLOGY (2011)

Letter Clinical Neurology

Autosomal dominant nemaline myopathy caused by a novel α-tropomyosin 3 mutation

I. C. Kiphuth et al.

JOURNAL OF NEUROLOGY (2010)

Article Genetics & Heredity

A novel nemaline myopathy in the Amish caused by a mutation in troponin T1

JJ Johnston et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2000)