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pro vyhledávání: '"Maisoon Alhamidi"'
Autor:
Maisoon Alhamidi, Elisabeth Kjeldsen Buvang, Toril Fagerheim, Vigdis Brox, Sigurd Lindal, Marijke Van Ghelue, Øivind Nilssen
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e22968 (2011)
Limb-Girdle Muscular Dystrophy type 2I (LGMD2I) is an inheritable autosomal, recessive disorder caused by mutations in the FuKutin-Related Protein (FKRP) gene (FKRP) located on chromosome 19 (19q13.3). Mutations in FKRP are also associated with Conge
Externí odkaz:
https://doaj.org/article/81cd612059c64b5cb2877c30251210fd
Publikováno v:
Neuromuscular disorders : NMD. 27(7)
Accepted manuscript version. Published version available at https://doi.org/10.1016/j.nmd.2017.02.015 . Limb girdle muscular dystrophy type 2I (LGMD2I) is a progressive disorder caused by mutations in the FuKutin-Related Protein gene (FKRP). LGMD2I d
Publikováno v:
Neuromuscular Disorders. 27:S109
Autor:
Vigdis Brox, Marijke Van Ghelue, Toril Fagerheim, Sigurd Lindal, Øivind Nilssen, Maisoon Alhamidi, Elisabeth Kjeldsen Buvang
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 8, p e22968 (2011)
PLoS ONE, Vol 6, Iss 8, p e22968 (2011)
Limb-Girdle Muscular Dystrophy type 2I (LGMD2I) is an inheritable autosomal, recessive disorder caused by mutations in the FuKutin-Related Protein (FKRP) gene (FKRP) located on chromosome 19 (19q13.3). Mutations in FKRP are also associated with Conge