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Authors: Lalwani, AK Goldstein, JA Kelley, MJ Luxford, W Castelein, CM Mhatre, AN

Citation: Ak. Lalwani et al., Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9, AM J HU GEN, 67(5), 2000, pp. 1121-1128

Authors: Lalwani, AK Castelein, CM

Citation: Ak. Lalwani et Cm. Castelein, Cracking the auditory genetic code: Nonsyndromic hereditary hearing impairment, AM J OTOL, 20(1), 1999, pp. 115-132

Authors: Lalwani, AK Luxford, WM Mhatre, AN Attaie, A Wilcox, ER Castelein, CM

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