Early onset autosomal dominant progressive muscular dystrophy presenting in childhood as a Becker phenotype—The importance of dystrophin and molecular genetic analysis-Reference-Cited by-同舟云学术

Early onset autosomal dominant progressive muscular dystrophy presenting in childhood as a Becker phenotype—The importance of dystrophin and molecular genetic analysis

Published:1992-01 Issue:2 Volume:2 Page:121-124
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Miller Geoffrey,Beggs Alan H.,Towfighi Javad

Publisher

Elsevier BV

Subject

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

Reference11 articles.

1. Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy;Gilchrist;Neurology,1988

2. Dystrophin characterization in muscle biopsies from Duchenne and Becker muscular dystrophy patients;Hoffman;N Engl J Med,1988

3. Multiplex PCR for the diagnosis of Duchenne muscular dystrophy;Chamberlain,1990

4. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction;Beggs;Hum Genet,1990

5. Father-to-son transmission of hemophilia A due to uniparietal disomy;Vidaud;Am J Hum Genet,1989

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1. Genetic epidemiology of Duchenne and Becker muscular dystrophy in Slovenia;Clinical Genetics;2008-06-28

2. Multiple bottlenecks in information processing? An electrophysiological examination;Psychonomic Bulletin & Review;2001-03

3. Inhibitory motor control in stop paradigms: review and reinterpretation of neural mechanisms;Acta Psychologica;1999-04

4. Limb girdle muscular dystrophy: A pathological and immunohistochemical reevaluation;Muscle & Nerve;1998-05

5. Childhood-onset autosomal-dominant limb-girdle muscular dystrophy with cardiac conduction block;Muscle & Nerve;1997-03