Publication | Closed Access
Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis☆
149
Citations
25
References
2003
Year
Signal TransductionGeneticsIon ChannelsGene FamilyMolecular GeneticsFunctional CluesDisease Gene IdentificationTransmembrane Channel-likeGene CharacterizationGene ExpressionMedicineCell BiologyCell SignalingCellular PhysiologyGene Function
| Year | Citations | |
|---|---|---|
1997 | 39.1K | |
1999 | 9K | |
2003 | 2K | |
1996 | 1.4K | |
2001 | 1.2K | |
1994 | 896 | |
2002 | 711 | |
Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23 Julie M. Bork, Linda Peters, Saima Riazuddin, The American Journal of Human Genetics Developmental BiologyAllelic MutationsMendelian DisorderGenetic DisorderGenetics | 2001 | 551 |
2002 | 501 | |
2002 | 471 |
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