Evidence for an autosomal recessive pattern of inheritance in Keratitis-ichthyosis-deafness (KID) syndrome: Exome sequencing reveals a novel homozygous GJB2 mutation
Journal article published in 2019 by
Khushnooda Ramzan 
,
Rozeena Huma,
Nouf S. Al-Numair ,
Faiqa Imtiaz,
Moeenaldeen Al-Sayed
,
Rozeena Huma,
Nouf S. Al-Numair ,
Faiqa Imtiaz,
Moeenaldeen Al-Sayed
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