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Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: Characterization of sub-clinical phenotypes

✍ Scribed by Angelini, C.; Fanin, M.; Pegoraro, E.; Freda, M.P.; Cadaldini, M.; Martinello, F.


Book ID
122007473
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
750 KB
Volume
4
Category
Article
ISSN
0960-8966

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## Communicated by Mireille Claustres Limb girdle muscular dystrophies (LGMD) are characterized by genetic and clinical heterogeneity: seven autosomal dominant and 12 autosomal recessive loci have so far been identified. Aims of this study were to evaluate the relative proportion of the different