Author:
Ahmed Zubair M,Cindy Li Xiaoyan,Powell Shontell D,Riazuddin Saima,Young Terry-Lynn,Ramzan Khushnooda,Ahmad Zahoor,Luscombe Sandra,Dhillon Kiran,MacLaren Linda,Ploplis Barbara,Shotland Lawrence I,Ives Elizabeth,Riazuddin Sheikh,Friedman Thomas B,Morell Robert J,Wilcox Edward R
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. Friedman TB, Griffith AJ: Human nonsyndromic sensorineural deafness. Annu Rev Genomics Hum Genet. 2003, 4: 341-402. 10.1146/annurev.genom.4.070802.110347.
2. Bonne-Tamir B, DeStefano AL, Briggs CE, Adair R, Franklyn B, Weiss S, Korostishevsky M, Frydman M, Baldwin CT, Farrer LA: Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3. Am J Hum Genet. 1996, 58: 1254-1259.
3. Veske A, Oehlmann R, Younus F, Mohyuddin A, Muller-Myhsok B, Mehdi SQ, Gal A: Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan. Hum Mol Genet. 1996, 5: 165-168. 10.1093/hmg/5.1.165.
4. Scott HS, Kudoh J, Wattenhofer M, Shibuya K, Berry A, Chrast R, Guipponi M, Wang J, Kawasaki K, Asakawa S, Minoshima S, Younus F, Mehdi SQ, Radhakrishna U, Papasavvas MP, Gehrig C, Rossier C, Korostishevsky M, Gal A, Shimizu N, Bonne-Tamir B, Antonarakis SE: Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness. Nat Genet. 2001, 27: 59-63.
5. Ben-Yosef T, Wattenhofer M, Riazuddin S, Ahmed ZM, Scott HS, Kudoh J, Shibuya K, Antonarakis SE, Bonne-Tamir B, Radhakrishna U, Naz S, Ahmed Z, Pandya A, Nance WE, Wilcox ER, Friedman TB, Morell RJ: Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness. J Med Genet. 2001, 38: 396-400. 10.1136/jmg.38.6.396.
Cited by
30 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献