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Hereditary protein C deficiency associated with riboflavin-responsive lipid storage myopathy

โœ Scribed by L. Vergani; C. Angelini; E. Pegoraro; M. Cadaldini; P. Simioni; A. Girolami; D.M. Turnbull


Book ID
115236105
Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
692 KB
Volume
3
Category
Article
ISSN
1351-5101

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linked to the phenotype in the families we have analyzed (manuscript in preparation). These observations may indicate that convulsions could be only one of the modes of expression of BFNC and BIFC mutant genes.