Clinical and genetic characterization of manifesting carriers of DMD mutations-Reference-Cited by-同舟云学术

Clinical and genetic characterization of manifesting carriers of DMD mutations

Published:2010-08 Issue:8 Volume:20 Page:499-504
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Soltanzadeh Payam,Friez Michael J.,Dunn Diane,von Niederhausern Andrew,Gurvich Olga L.,Swoboda Kathryn J.,Sampson Jacinda B.,Pestronk Alan,Connolly Anne M.,Florence Julaine M.,Finkel Richard S.,Bönnemann Carsten G.,Medne Livija,Mendell Jerry R.,Mathews Katherine D.,Wong Brenda L.,Sussman Michael D.,Zonana Jonathan,Kovak Karen,Gospe Sidney M.,Gappmaier Eduard,Taylor Laura E.,Howard Michael T.,Weiss Robert B.,Flanigan Kevin M.

Publisher

Elsevier BV

Subject

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

Reference28 articles.

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3. Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy;Taylor;J Med Genet,2007

4. Mosaic expression of dystrophin in symptomatic carriers of Duchenne’s muscular dystrophy;Arahata;N Engl J Med,1989

5. Dystrophinopathy in isolated cases of myopathy in females;Hoffman;Neurology,1992

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