LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss
- Resource Type
- Article
- Authors
- Al-Amri, Ahmed H.; Al Saegh, Abeer; Al-Mamari, Watfa; El-Asrag, Mohammed E.; Al-Kindi, Mohammed N.; Al Khabouri, Mazin; Al Wardy, Nadia; Al Lamki, Khalsa; Gabr, Ahlam; Idris, Ahmed; Inglehearn, Chris F.; Clapcote, Steven J.; Ali, Manir
- Source
- In European Journal of Medical Genetics December 2019 62(12)
- Subject
- Language
- ISSN
- 1769-7212