Paula B. Andrade

Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p

Atteeq U. Rehman, Khitab Gul, Robert J. Morell et al. · Human Genetics · 2011 · 58 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +6

Novel <i>CLDN14</i> mutations in Pakistani families with autosomal recessive non‐syndromic hearing loss

Kwanghyuk Lee, Muhammad Ansar, Paula B. Andrade et al. · American Journal of Medical Genetics Part A · 2012 · 26 citations · Full text

DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2

Sulman Basit, Kwanghyuk Lee, Rabia Habib et al. · Human Genetics · 2010 · 23 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +10

Novel <i>TMPRSS3</i> variants in Pakistani families with autosomal recessive non‐syndromic hearing impairment

Kwanghyuk Lee, Saad Ullah Khan, Abul Bashar Mir Md. Khademul Islam et al. · Clinical Genetics · 2011 · 16 citations · Full text