Autosomal-Recessive Hearing Impairment due to Rare Missense Variants within S1PR2

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Autosomal-Recessive Hearing Impairment due to Rare Missense Variants within S1PR2 Empty Autosomal-Recessive Hearing Impairment due to Rare Missense Variants within S1PR2

Post  Jon Moulton on Wed Jan 27, 2016 9:11 am

Santos-Cortez RL, Faridi R, Rehman AU, Lee K, Ansar M, Wang X, Morell RJ, Isaacson R, Belyantseva IA, Dai H, Acharya A, Qaiser TA, Muhammad D, Ali RA, Shams S, Hassan MJ, Shahzad S, Raza SI, Bashir ZE, Smith JD, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics, Riazuddin S, Ahmad W, Friedman TB, Leal SM. Autosomal-Recessive Hearing Impairment due to Rare Missense Variants within S1PR2. Am J Hum Genet. 2016 Jan 19. pii: S0002-9297(15)00499-1. doi: 10.1016/j.ajhg.2015.12.004. [Epub ahead of print]
Jon Moulton
Jon Moulton

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