A study of possible heterogeneity in Duchenne muscular dystrophy
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1979.tb01777.x/fullpdf
Reference23 articles.
1. Amino acids of plasma and urine in diseases of muscle;Bank;Arch. Neurol.,1971
2. Serum lactate dehydrogenase isoenzyme 5 (LDH-5) in carriers of Duchenne muscular dystrophy;Burt;Neurology,1979
3. The genetic relationship of progressive muscular dystrophy (Duchenne type) and mental retardation;Cohen;Develop. Med. Child Neurol.,1968
4. Estimation of the proportion of new mutants amongst cases of Duchenne muscular dystrophy;Davie;J. med. Genet.,1978
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