Genetic and Early Clinical Manifestations of Females Heterozygous for Duchenne/Becker Muscular Dystrophy-Reference-Cited by-同舟云学术

Genetic and Early Clinical Manifestations of Females Heterozygous for Duchenne/Becker Muscular Dystrophy

Published:2016-02 Issue: Volume:55 Page:58-63
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Papa Riccardo,Madia Francesca,Bartolomeo Domenico,Trucco Federica,Pedemonte Marina,Traverso Monica,Broda Paolo,Bruno Claudio,Zara Federico,Minetti Carlo,Fiorillo Chiara

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference10 articles.

1. The manifesting carrier in Duchenne muscular dystrophy;Moser;Clin Genet,1974

2. A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales;Norman;Clin Genet,1989

3. Clinical and genetic characterization of manifesting carriers of DMD mutations;Soltanzadeh;Neuromuscul Disord,2010

4. Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age;Mercier;Eur J Hum Genet,2013

5. Diagnostic and clinical characteristics of early- manifesting females with Duchenne or Becker muscular dystrophy;Imbornoni;Am J Med Genet A,2014

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