Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes

By Bi Weimin   Yan Jiong   Shi Xin   Yuva-Paylor Lisa A.   Antalffy Barbara A.   Goldman Alica   Yoo Jong W.   Noebels Jeffrey L.   Armstrong Dawna L.   Paylor Richard   Lupski James R.  

Human Molecular Genetics, Vol. 16, Iss. 15, 2007-08 ,pp. : 1802-1813

Oxford University Press

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Caveolin-3 deficiency causes muscle degeneration in mice

By Hagiwara Yasuko   Sasaoka Toshikuni   Araishi Kenji   Imamura Michihiro   Yorifuji Hiroshi   Nonaka Ikuya   Ozawa Eijiro   Kikuchi Tateki  

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Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

By Teubner Barbara  

Human Molecular Genetics, Vol. 12, Iss. 1, 2003-01 ,pp. : 13-21

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Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice

By Beck Tyler F.   Veenma Danielle   Shchelochkov Oleg A.   Yu Zhiyin   Kim Bum Jun   Zaveri Hitisha P.   van Bever Yolande   Choi Sunju   Douben Hannie   Bertin Terry K.   Patel Pragna I.   Lee Brendan   Tibboel Dick   de Klein Annelies   Stockton David W.   Justice Monica J.   Scott Daryl A.  

Human Molecular Genetics, Vol. 22, Iss. 5, 2013-03 ,pp. : 1026-1038

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LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice

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Human Molecular Genetics, Vol. 12, Iss. 6, 2003-03 ,pp. : 631-646

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