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Details on Person Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

Class:IdLiteratureReference:9664089
_displayNameMutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus
_timestamp2019-10-21 10:49:42
author[Person:9650536] Verpy, E
[Person:9664123] Masmoudi, S
[Person:9664016] Zwaenepoel, I
[Person:9664069] Leibovici, M
[Person:9664155] Hutchin, T P
[Person:9664120] Del Castillo, I
[Person:9664125] Nouaille, S
[Person:9664083] Blanchard, S
[Person:9664045] Lainé, S
[Person:9664157] Popot, J L
[Person:9664086] Moreno, F
[Person:9664127] Mueller, R F
[Person:9664034] Petit, C
created[InstanceEdit:9664104] May, Bruce, 2019-10-21
journalNat. Genet.
pages345-9
pubMedIdentifier11687802
titleMutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus
volume29
year2001
(literatureReference)[RegulationReference:9664002] Requirement by 'Strc [plasma membrane]' Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus
[RegulationReference:9671855] Requirement by 'Strc:Otog:Otogl [extracellular region]' Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane
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