List of works - Morad Khayat - Paulina

List of works by Morad Khayat

A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis ⬇️

scientific article published on June 20, 2012

A homozygous TTN gene variant associated with lethal congenital contracture syndrome

scientific article published on 01 April 2018

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

scientific article published on 24 August 2020

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