Sporadic occurrence of Duchenne Muscular Dystrophy: evidence for new mutation-Reference-Cited by-同舟云学术

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Sporadic occurrence of Duchenne Muscular Dystrophy: evidence for new mutation

Published:2008-06-28 Issue:5 Volume:18 Page:329-341
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Caskey C. Thomas,Nussbaum Robert L.,Cohan Leslie C.,Pollack Lynda

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1980.tb02293.x/fullpdf

Reference41 articles.

1. Detection of Fabry's disease heterozygotes by hair root analysis;Beaudet;Clin. Genet.,1978

2. The sporadic case of hemophilia A;Biggs;Lancer,1976

3. Studies on hair roots for car rier detection in hypoxanthine-guanine phosphoribosyl transferase deficiency;Bruyn;Clin. Genet.,1974

4. Serum LDH-J in carriers of Duchenne muscular dystrophy;Burt;Neurology,1978

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1. Estimated costs for Duchenne muscular dystrophy care in Brazil;Orphanet Journal of Rare Diseases;2023-06-22

2. Estimated Costs for Duchenne Muscular Dystrophy Care in Brazil;2023-03-15

3. Matrilineal analysis of mutations in the DMD gene in a multigenerational South Indian cohort using DMD gene panel sequencing;Molecular Genetics & Genomic Medicine;2021-05-07

4. Duchenne muscular dystrophy;Nature Reviews Disease Primers;2021-02-18

5. Duchenne and Becker muscular dystrophy carriers: Evidence of cardiomyopathy by exercise and cardiac MRI testing;International Journal of Cardiology;2020-10

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