Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice

By Dixon Michael J.   Gazzard James  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1579-1584

Oxford University Press

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Targeted disruption of Slc19a2 , the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice

By Forrest D.  

Human Molecular Genetics, Vol. 11, Iss. 23, 2002-11 ,pp. : 2951-2960

Oxford University Press

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Organization and expression of the SLC36 cluster of amino acid transporter genes

By Bermingham John  

Mammalian Genome, Vol. 15, Iss. 2, 2004-02 ,pp. : 114-125

Springer Publishing Company

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Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis

By Campeau Philippe M.   Lu James T.   Sule Gautam   Jiang Ming-Ming   Bae Yangjin   Madan Simran   Högler Wolfgang   Shaw Nicholas J.   Mumm Steven   Gibbs Richard A.   Whyte Michael P.   Lee Brendan H.  

Human Molecular Genetics, Vol. 21, Iss. 22, 2012-11 ,pp. : 4904-4909

Oxford University Press

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Genetic variation in the human urea transporter-2 is associated with variation in blood pressure

By Chen Y-D.I.  

Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2157-2164

Oxford University Press

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