A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment

By Rhodes Charlotte  

Mammalian Genome, Vol. 15, Iss. 9, 2004-09 ,pp. : 686-697

Springer Publishing Company

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Usher syndromes due to MYO7A , PCDH15 , USH2A or GPR98 mutations share retinal disease mechanism

By Jacobson Samuel G.   Cideciyan Artur V.   Aleman Tomas S.   Sumaroka Alexander   Roman Alejandro J.   Gardner Leigh M.   Prosser Haydn M.   Mishra Monalisa   Bech-Hansen N. Torben   Herrera Waldo   Schwartz Sharon B.   Liu Xue-Zhong   Kimberling William J.   Steel Karen P.   Williams David S.  

Human Molecular Genetics, Vol. 17, Iss. 15, 2008-08 ,pp. : 2405-2415

Oxford University Press

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Characterization of Unconventional MYO6 , the Human Homologue of the Gene Responsible for Deafness in Snell's Waltzer Mice

By Avraham Karen B.  

Human Molecular Genetics, Vol. 6, Iss. 8, 1997-01 ,pp. : 1225-1231

Oxford University Press

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The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5a

By Jones Julie M.  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 821-828

Oxford University Press

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Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration

By Melcon Gisela   Kozlov Serguei   Hernandez Lidia   Zhao Po   Mitchell Stephanie   Nader Gustavo   Bakay Marina   Rottman Jeff N.   Hoffman Eric P.   Stewart Colin L.  

Human Molecular Genetics, Vol. 15, Iss. 4, 2006-02 ,pp. : 637-651

Oxford University Press

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