Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader–Willi syndrome

Author： Tsai Ting-Fen   Jiang Yong-hui   Bressler Jan   Armstrong Dawna   Beaudet Arthur L.   Jiang Y.   Lalande M.   Nicholls R.D.   Malzac P.   Fang P.   Cassidy S.B.   Saitoh S.   Leff S.E.   Özçelik T.   Cattanach B.M.   Yang T.   McAllister G.   Schmauss C.   Sun Y.   Kuslich C.D.   Schulze A.   Conroy J.M.   Gabriel J.M.   Glenn C.C.   Shemer R.   Sutcliffe J.S.   Zeschnigk M.   Ramirez-Solis R.   Jiang Y.-H.   Watrin F.   Albrecht U.   Johnson D.K.   McMahon A.P.   Ramirez-Solis R.   Ramirez-Solis R.   Sambrook J.   Wevrick R.   Wagstaff J.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.8, Iss.8, 1999-08, pp. : 1357-1364

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