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Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.
Cell. 2001 Jan 12;104(1):165-72. doi: 10.1016/s0092-8674(01)00200-8.
Cell. 2001.
PMID: 11163249
Free article.
Dominant modifier DFNM1 suppresses recessive deafness DFNB26.
Riazuddin S, Castelein CM, Ahmed ZM, Lalwani AK, Mastroianni MA, Naz S, Smith TN, Liburd NA, Friedman TB, Griffith AJ, Riazuddin S, Wilcox ER.
Riazuddin S, et al. Among authors: liburd na.
Nat Genet. 2000 Dec;26(4):431-4. doi: 10.1038/82558.
Nat Genet. 2000.
PMID: 11101839
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Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.
Liburd N, Ghosh M, Riazuddin S, Naz S, Khan S, Ahmed Z, Riazuddin S, Liang Y, Menon PS, Smith T, Smith AC, Chen KS, Lupski JR, Wilcox ER, Potocki L, Friedman TB.
Liburd N, et al.
Hum Genet. 2001 Nov;109(5):535-41. doi: 10.1007/s004390100604. Epub 2001 Oct 3.
Hum Genet. 2001.
PMID: 11735029
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