Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment - Kakar, Mohib Ullah; Akram, Muhammad; Zubair Mehboob, Muhammad; Younus, Muhammad; Bilal, Muhammad; Waqas, Ahmed; Nazir, Amina; Shafi, Muhammad; Umair, Muhammad; Ahmad, Sajjad; Rafeeq, Misbahuddin M. (PloS one, 2022)
Keywords: Amino acids; Auditory system; Biology and life sciences; Causes of; Chromosome 19; CRISPR; Deafness; DNA sequencing; Ears & hearing; Gene silencing; Gene therapy; Genes; Genetic aspects; Genetic modification; Genetic variation; Genome editing; Hearing; Hearing loss; Impairment; Medical research; Medicine and Health Sciences; Medicine, Experimental; Nucleotide sequencing; Proteins; RNA editing; RNA-mediated interference; SIX gene family; Pakistan; United States--US; Afghanistan