Mutations in BICD2, which encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy

Authors :: Neveling, K.
Martinez-Carrera, L.
Hölker, I.
Heister, A.
Verrips, A.
Hosseini-Barkooie, S.M.
Gilissen, C.F.H.A.
Vermeer, S.
Pennings, M.C.P.
Meijer, R.
Riele, M.G.E. te
Frijns, C.J.
Suchowersky, O.
MacLaren, L.
Rudnik-Schöneborn, S.
Sinke, R.J.
Zerres, K.
Lowry, R.B.
Lemmink, H.H.
Garbes, L.
Veltman, J.A.
Schelhaas, H.J.
Scheffer, H.
Wirth, B.
Neveling, K.
Martinez-Carrera, L.
Hölker, I.
Heister, A.
Verrips, A.
Hosseini-Barkooie, S.M.
Gilissen, C.F.H.A.
Vermeer, S.
Pennings, M.C.P.
Meijer, R.
Riele, M.G.E. te
Frijns, C.J.
Suchowersky, O.
MacLaren, L.
Rudnik-Schöneborn, S.
Sinke, R.J.
Zerres, K.
Lowry, R.B.
Lemmink, H.H.
Garbes, L.
Veltman, J.A.
Schelhaas, H.J.
Scheffer, H.
Wirth, B.
Source :: American Journal of Human Genetics; 946; 954; 0002-9297; vol. 92; ~American Journal of Human Genetics~946~954~~~0002-9297~~92~~
Publication Year :: 2013
Abstract: Contains fulltext : 116576.pdf (publisher's version ) (Closed access)

Database :: OAIster
Journal :: American Journal of Human Genetics; 946; 954; 0002-9297; vol. 92; ~American Journal of Human Genetics~946~954~~~0002-9297~~92~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1284032361
Document Type :: Electronic Resource

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