Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans

By Zheng Qing Yin  

Human Molecular Genetics, Vol. 14, Iss. 1, 2005-01 ,pp. : 103-111

Oxford University Press

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Myosin VIIA Gene: Heterogeneity of the Mutations Responsible for Usher Syndrome Type IB

By Lévy Gallia   Levi-Acobas Fabienne   Blanchard Stéphane   Gerber Sylvie   Larget-Piet Dominique   Chenal Viviane   Liu Xue-Zhong   Newton Valerie   Steel Karen P.   Brown Steve D. M.   Munnich Arnold   Kaplan Josseline   Petit Christine   Weil Dominique  

Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 111-116

Oxford University Press

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Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids

By Bahloul Amel   Michel Vincent   Hardelin Jean-Pierre   Nouaille Sylvie   Hoos Sylviane   Houdusse Anne   England Patrick   Petit Christine  

Human Molecular Genetics, Vol. 19, Iss. 18, 2010-09 ,pp. : 3557-3565

Oxford University Press

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Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis

By Merryweather-Clarke Alison T.  

Human Molecular Genetics, Vol. 12, Iss. 17, 2003-09 ,pp. : 2241-2247

Oxford University Press

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Mariner is defective in myosin VIIA : a zebrafish model for human hereditary deafness

By Ernest Sylvain   Rauch Gerd-Jörg  

Human Molecular Genetics, Vol. 9, Iss. 14, 2000-09 ,pp. : 2189-2196

Oxford University Press

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