Genetics of congenital nemaline myopathy: a study of 10 families.

Author:

Wallgren-Pettersson C,Kaariainen H,Rapola J,Salmi T,Jaaskelainen J,Donner M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference31 articles.

1. Light and electron microscopic studies of 'myogranules" in a child with hypotonia and muscle weakness;Conen, P.E.; Murphy, E.G.; Donohue, W.L.;Can Med Assoc

2. Childhood nemaline myopathy: a review of clinical presentation in relation to prognosis. D)ev AJed;Martinez, B.A.; Lake, B.D.;(Child Neurol,1987

3. Late-onset rod nyvopathv: a niewlv recognized, acquired, and progressive disease;Engel, W.K.; Resnick, J.S.;Neurology,1966

4. Neinalinie mvopathy: comparatiVe muscle histochemistry in the scvere neonatal, moderate conigenital, and adult-onset McKusick VA. Mendelian forms. Iediatr Neurol 1989; 5: 25-3 1. itnherioance in matn. Caialogs ol-atlosoinal dominant, autosomal recessive, and X-linked phenotypc'es;I, Shimomura C.Nonaka

5. Nemaline myopathy. A longterm clinicopathologic study of affected mother and daughter;Brain,1966

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