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Correlation of clinical function and muscle CT scan images in limb-girdle muscular dystrophy

✍ Scribed by M. Vlak *, † , E. van der Kooi; C. Angelini

Publisher
Springer Milan
Year
2000
Tongue
English
Weight
33 KB
Volume
21
Category
Article
ISSN
1590-1874

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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