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pro vyhledávání: '"Waleed M. Al-Maneea"'
Autor:
Waleed M. Al-Maneea, Mustafa A. Salih, Louis M. Kunkel, Anna R. Duncan, M.Z. Seidahmed, Hisham Alkhalidi, Salem H. Alshemmari, Stephanie L. Burgess, Abdullah S. Al-Jarallah, Steven E. Boyden, Richard R. Bennett, Elicia Estrella, Peter B. Kang, Alexander J. White
Publikováno v:
Neurogenetics
Limb girdle muscular dystrophy type 2 (LGMD2) is a genetically heterogeneous autosomal recessive disorder caused by mutations in 15 known genes. DNA sequencing of all candidate genes can be expensive and laborious, whereas a selective sequencing appr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f15137f2fe10414451ff7375d4b4cfa
https://doi.org/10.1007/s10048-010-0250-9
https://doi.org/10.1007/s10048-010-0250-9
