Duchenne muscular dystrophy: Gene and gene product; mechanism of mutation in the gene
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799613
Reference16 articles.
1. Brooke MH, Fenichel GM, Griggs RC et al (1989). Duchenne muscular dystrophy: Patterns of clinical progression and effects of supportive therapy.Neurology 39:475–481.
2. Bodrug SE, Ray PN, Gonzalez IL, Schmickel RD, Sylvester JE, Worton RG (1987). Molecular analysis of a constitutional X-autosomal translocation in a female with muscular dystrophy.Science 237:1620–1624.
3. Bodrug SE, Burghes AHM, Ray PN, Worton RG (1989). Fine mapping of four constitutive translocations at the 5′ end of the Duchenne muscular dystrophy gene.Genomics 4:101–104.
4. Bodrug SE, Holden JJA, Ray PN, Worton RG (1991). Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.EMBO J 10:3931–3939.
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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