Mutations in the sarcoglycan genes cause autosomalrecessive muscular dystrophies. Because sarcoglycan genes and their protein products are highly expressed both in skeletal and cardiac muscle, patients with these mutations might be expected to be at risk to develop dilated cardiomyopathy. We therefo
β¦ LIBER β¦
Analysis of muscular dystrophies gene mutations in Southern Italy
β Scribed by L. Politano; V. Nigro
- Book ID
- 116168827
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 114 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0960-8966
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Heart involvement in muscular dystrophie
β
P. Melacini; M. Fanin; D.J. Duggan; M.P. Freda; A. Berardinelli; G.A. Danieli; A
π
Article
π
1999
π
John Wiley and Sons
π
English
β 320 KB
π 1 views
Mutation analysis in emery-dreifuss musc
β
Yoram Nevo; Mohammed Al-Lozi; Alexander Sh Parsadanian; Jeffrey L Elliott; Anne
π
Article
π
1999
π
Elsevier Science
π
English
β 92 KB
Analysis of HFE gene mutations in a popu
β
T. Restuccia; S. Campo; D. Villari; G. Raffa; D. Cucinotta; G. Squadrito; T. Pol
π
Article
π
2000
π
Elsevier Science
π
English
β 122 KB
Duchenne muscular dystrophy: Gene and ge
β
R. G. Worton
π
Article
π
1992
π
Springer
π
English
β 1012 KB
Fukutin gene mutations in steroid-respon
β
Caroline Godfrey; Diana Escolar; Martin Brockington; Emma M. Clement; Rachael Me
π
Article
π
2006
π
John Wiley and Sons
π
English
β 503 KB
## 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
Neurocognitive Profiles in Duchenne Musc
β
Maria Grazia DβAngelo; Maria Luisa Lorusso; Federica Civati; Giacomo Pietro Comi
π
Article
π
2011
π
Elsevier Science
π
English
β 518 KB