## Abstract ## Objective Defects in glycosylation of Ξ±βdystroglycan are associated with several forms of muscular dystrophy, often characterized by congenital onset and severe structural brain involvement, collectively known as dystroglycanopathies. Six causative genes have been identified in thes
β¦ LIBER β¦
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes
β Scribed by Roberta Biancheri; Antonio Falace; Alessandra Tessa; Marina Pedemonte; Sara Scapolan; Denise Cassandrini; Chiara Aiello; Andrea Rossi; Paolo Broda; Federico Zara; Filippo Maria Santorelli; Carlo Minetti; Claudio Bruno
- Book ID
- 116295711
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 483 KB
- Volume
- 363
- Category
- Article
- ISSN
- 0006-291X
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