Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiency-Reference-Cited by-同舟云学术

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Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiency

Published:1997-10 Issue: Volume:7 Page:S57-S62
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Porschke H.,Kress W.,Reichmann H.,Goebel H.H.,Grimm T.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference28 articles.

1. Die oculopharyngeale Muskeldystrophie;Hartmann;Nervenarzt,1979

2. Bericht über eine Großfamilie mit okulopharyngealer Muskeldystrophie;Engelhardt,1989

3. Okulopharyngeale Muskeldystrophie;Klostermann;Nervenarzt,1990

4. An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement;Schmitt;Muscle Nerve,1981

5. Oculopharyngeal muscular dystrophy;Little;J Neurol Sci,1982

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4. Distrofia muscolare oculofaringea;EMC - Neurologia;2017-02

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