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LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss

Document Type

Article

Author

Al-Amri, A.H.; El-Asrag, M.E.; Inglehearn, C.F.; Ali, M.; Clapcote, S.J.; Al Saegh, A.; Al-Mamari, W.; Gabr, A.; Idris, A.; Al-Kindi, M.N.; Al Wardy, N.; Al Lamki, K.; Al Khabouri, M.

Source

In: European Journal of Medical Genetics. (European Journal of Medical Genetics, December 2019, 62(12))

Subject

Language

English

ISSN

18780849
17697212

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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