Mutations in thelipoma HMGIC fusion partner-like 5 (LHFPL5)gene cause autosomal recessive nonsyndromic hearing loss-Reference-Cited by-同舟云学术

Mutations in thelipoma HMGIC fusion partner-like 5 (LHFPL5)gene cause autosomal recessive nonsyndromic hearing loss

Published:2006-07 Issue:7 Volume:27 Page:633-639
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Kalay Ersan,Li Yun,Uzumcu Abdullah,Uyguner Oya,Collin Rob W.,Caylan Refik,Ulubil-Emiroglu Melike,Kersten Ferry F.J.,Hafiz Gunter,van Wijk Erwin,Kayserili Hulya,Rohmann Edyta,Wagenstaller Janine,Hoefsloot Lies H.,Strom Tim M.,Nürnberg Gudrun,Baserer Nermin,den Hollander Anneke I.,Cremers Frans P.M.,Cremers Cor W.R.J.,Becker Christian,Brunner Han G.,Nürnberg Peter,Karaguzel Ahmet,Basaran Seher,Kubisch Christian,Kremer Hannie,Wollnik Bernd

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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2. Molecular Specializations Underlying Phenotypic Differences in Inner Ear Hair Cells of Zebrafish and Mice;2024-05-26

3. LHFPL5 is a key element in force transmission from the tip link to the hair cell mechanotransducer channel;Proceedings of the National Academy of Sciences;2024-01-09

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