Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy-Reference-Cited by-同舟云学术

Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy

Published:1999-05 Issue:3 Volume:9 Page:166-170
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Hoeltzenbein Maria,Karow Thomas,Zeller Joern A,Warzok Rolf,Wulff Karin,Zschiesche Marlies,Herrmann Falko H,Große-Heitmeyer Wolfgang,Wehnert Manfred S

Publisher

Elsevier BV

Subject

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

Reference10 articles.

1. McKusick VA. Mendelian Inheritance in Man. Catalogs of Human Genes and Genetic Disorders, tenth ed. Baltimore, MD: Johns Hopkins University Press, 1994:1926–1928.

2. Unusual type of a benign X-linked muscular dystrophy;Emery;J Neurol Neurosurg Psychiatry,1966

3. Yates JRW. Emery–Dreifuss muscular dystrophy. In: Emery AEH, editor. Diagnostic criteria for neuromuscular disorders, second ed. London: Royal Society of Medicine Press, 1997:5–8.

4. Emery–Dreifuss syndrome;Emery;J Med Genet,1989

5. Emery–Dreifuss humeroperoneal muscular dystrophy: an X-linked myopathy with unusual contractures and bradycardia;Hopkins;Ann Neurol,1981

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