Genetic and clinical correlations of Xp21 muscular dystrophy
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799614
Reference41 articles.
1. Becker PE (1962) Two new families of benign sex-linked recessive muscular dystrophy.Rev Can Biol 21: 551–566.
2. Becker PE, Kiener F (1955) Eine neue X-chromosome muskeldystrophie.Arch Psychiatr Z Neurol 193: 427–448.
3. Boyce FM, Beggs AH, Feener C, Kunkel LM (1991) Dystrophin is transcribed in brain from a distant upstream promoter.Proc Natl Acad Sci USA 88: 1276–1280.
4. Brooke MH, Fenichel GM, Griggs RC et al (1983) Clinical investigation in Duchenne dystrophy: 2. Determination of the ‘power’ of therapeutic trials based on the natural history.Muscle Nerve 6: 91–103.
5. Bulman DE, Gangopadhyay SB, Bebchuck KG, Worton RG, Ray PN (1991) Point mutation in the human dystrophin gene: identification through western blot analysis.Genomics 10: 457–460.
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