Publications
Export 2 results:
Author Title [ Year
] Filters: Author is Rehman, Atteeq U and Keyword is Amino Acid Sequence [Clear All Filters]
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2. Am J Hum Genet 98, 331-8 (2016).
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. Am J Hum Genet 94, 144-52 (2014).
