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1 Ergebnisse
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LHFPL5 mutation: A rare cause of non-syndromic autosomal re..:
Al-Amri, Ahmed H.
;
Al Saegh, Abeer
;
Al-Mamari, Watfa
...
European Journal of Medical Genetics. 62 (2019) 12 - p. 103592 , 2019
Link:
https://doi.org/10.1016/j.ejmg.2018.11.026
RT Journal T1
LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ejmg.2018.11.026&Exemplar=1&LAN=DE A1 Al-Amri, Ahmed H. A1 Al Saegh, Abeer A1 Al-Mamari, Watfa A1 El-Asrag, Mohammed E. A1 Al-Kindi, Mohammed N. A1 Al Khabouri, Mazin A1 Al Wardy, Nadia A1 Al Lamki, Khalsa A1 Gabr, Ahlam A1 Idris, Ahmed A1 Inglehearn, Chris F. A1 Clapcote, Steven J. A1 Ali, Manir PB Elsevier BV YR 2019 SN 1769-7212 JF European Journal of Medical Genetics VO 62 IS 12 SP 103592 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2018.11.026 DO https://doi.org/10.1016/j.ejmg.2018.11.026 SF ELIB - SuUB Bremen
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