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Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy

✍ Scribed by H. B. Ginjaar; A. J. van der Kooi; H. Ceelie; A. L. J. Kneppers; M. van Meegen; P. G. Barth; H. F. M. Busch; J. H. J. Wokke; L. V. B. Anderson; C. G. Bönnemann; M. Jeanpierre; P. A. Bolhuis; A. F. M. Moorman; M. de Visser; E. Bakker; G. J. B. v. Ommen


Publisher
Springer
Year
2000
Tongue
English
Weight
965 KB
Volume
247
Category
Article
ISSN
0340-5354

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We report childhood-onset autosomal-dominant limb-girdle muscular dystrophy (LGMD) in a Chinese family with complete atrioventricular conduction block in the adult members. Six patients, including 5 men and 1 woman with an age of onset from 3 to 7 years, were affected. The grandfather had exercise i