Related content

Mutations in the Wolfram syndrome 1 gene ( WFS1 ) are a common cause of low frequency sensorineural hearing loss

By Kurnool P.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2501-2508

Oxford University Press

Access to resources Recommend Favorite

Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

By Fukuoka Hisakuni   Kanda Yukihiko   Ohta Shuji   Usami Shin-ichi  

Journal of Human Genetics, Vol. 52, Iss. 6, 2007-06 ,pp. : 510-515

Springer Publishing Company

Access to resources Recommend Favorite

De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia

By Brin M.F.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1133-1136

Oxford University Press

Access to resources Recommend Favorite

Two imprinted gene mutations: three phenotypes

By Cattanach Bruce M.   Peters Josephine   Ball Simon   Rasberry Carol  

Human Molecular Genetics, Vol. 9, Iss. 15, 2000-09 ,pp. : 2263-2273

Oxford University Press

Access to resources Recommend Favorite

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene

By Johnson Kenneth R.   Gagnon Leona H.   Webb Lisa S.   Peters Luanne L.   Hawes Norman L.   Chang Bo   Zheng Qing Yin  

Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3075-3086

Oxford University Press

Access to resources Recommend Favorite