| 1 | DIS, DFNB16, STRC, CATSPER2
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| Sensorineural deafness and male infertility: a contiguous gene deletion syndrome.
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| Zhang Y, Malekpour M, Al-Madani N, Kahrizi K, Zanganeh M, Mohseni M, Mojahedi F, Daneshi A, Najmabadi H, Smith RJ.
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| J Med Genet 44(4):233-40. Epub 2006 Nov 10. 2007
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| 2 | DIS, DFNB16, STRC, CATSPER2, HISPPD2B, CATSPER2P1
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| CATSPER2, a human autosomal nonsyndromic male infertility gene.
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| Avidan N, Tamary H, Dgany O, Cattan D, Pariente A, Thulliez M, Borot N, Moati L, Barthelme A, Shalmon L, Krasnov T, Ben-Asher E, Olender T, Khen M, Yaniv I, Zaizov R, Shalev H, Delaunay J, Fellous M, Lancet D, Beckmann JS.
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| Eur J Hum Genet 11(7):497-502. 2003
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| 3 | DFNB16, STRC
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| Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus.
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| Verpy E, Masmoudi S, Zwaenepoel I, Leibovici M, Hutchin TP, Del Castillo I, Nouaille S, Blanchard S, Laine S, Popot JL, Moreno F, Mueller RF, Petit C.
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| Nat Genet 29(3):345-9. 2001
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| 4 | STRC
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| A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss(DFNB16) maps to human chromosome 15q21-q22.
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| Campbell DA, McHale DP, Brown KA, Moynihan LM, Houseman M, Karbani G,Parry G, Janjua AH, Newton V, al-Gazali L, Markham AF, Lench NJ, Mueller RF.
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| J Med Genet 34(12):1015-7. 1997
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