Diagnosis of DMD Carrier Status in a Family with No Known Affected Males-Reference-Cited by-同舟云学术

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Diagnosis of DMD Carrier Status in a Family with No Known Affected Males

Published:2008-11-12 Issue:1 Volume:35 Page:70-73
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Muntoni F.,Mateddu A.,Cau M.,Congiu R.,Puddu R.,Cossu P.,Cao A.,Melis M. A.

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1993.tb11554.x/fullpdf

Reference19 articles.

1. Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide;Arahata;Nature,1988

2. Mosaic expression of dystrophin in symptomatic carriers of Duchenne muscular dystrophy;Arahata;New England Journal of Medicine,1989

3. Normal and dystrophin deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy;Bonilla;American Journal of Pathology,1988

4. Partial dystrophin deficiency in monozygous twin carriers discordant for clinical myopathy;Bonilla;Neurology,1990

5. The regeneration of skeletal muscle fibers following injury: a review;Carlson;Medicine and Science in Sport and Exercise,1983

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