TMC2 (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "TMC2" in Arabic language version.

Last modified: 22:44:00, 2 February 2025 (UTC)

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Kurima K، Peters LM، Yang Y، Riazuddin S، Ahmed ZM، Naz S، Arnaud D، Drury S، Mo J، Makishima T، Ghosh M، Menon PS، Deshmukh D، Oddoux C، Ostrer H، Khan S، Riazuddin S، Deininger PL، Hampton LL، Sullivan SL، Battey JF Jr، Keats BJ، Wilcox ER، Friedman TB، Griffith AJ (مارس 2002). "Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function". Nat Genet. ج. 30 ع. 3: 277–84. DOI:10.1038/ng842. PMID:11850618.
Kurima K، Yang Y، Sorber K، Griffith AJ (أغسطس 2003). "Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis". Genomics. ج. 82 ع. 3: 300–8. DOI:10.1016/S0888-7543(03)00154-X. PMID:12906855.

Kurima K، Peters LM، Yang Y، Riazuddin S، Ahmed ZM، Naz S، Arnaud D، Drury S، Mo J، Makishima T، Ghosh M، Menon PS، Deshmukh D، Oddoux C، Ostrer H، Khan S، Riazuddin S، Deininger PL، Hampton LL، Sullivan SL، Battey JF Jr، Keats BJ، Wilcox ER، Friedman TB، Griffith AJ (مارس 2002). "Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function". Nat Genet. ج. 30 ع. 3: 277–84. DOI:10.1038/ng842. PMID:11850618.
Kurima K، Yang Y، Sorber K، Griffith AJ (أغسطس 2003). "Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis". Genomics. ج. 82 ع. 3: 300–8. DOI:10.1016/S0888-7543(03)00154-X. PMID:12906855.