Lymphocyte capping in limb-girdle muscular dystrophy
β Scribed by Sybert, Virginia P. ;Bader, Patricia I. ;Townsend, Douglas W. ;Conn, Patricia S.
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 161 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0148-7299
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## 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
Ninety-seven muscle biopsies from 81 limb girdle muscular dystrophy (LGMD) patients [32 autosomal recessive (AR), 15 autosomal dominant (AD), 34 sporadic] were morphologically reevaluated. Sarcoglycan analysis was done in 37 available muscle biopsies of AR and sporadic patients. Chi-square tests wer