Characterization of a spontaneous, recessive, missense mutation arising in the Tecta gene.

Characterization of a spontaneous, recessive, missense mutation arising in the Tecta gene.

Item
http://www.wikidata.org/entity/Q36824671
Mammalian Otolin: a multimeric glycoprotein specific to the inner ear that interacts with otoconial matrix protein Otoconin-90 and Cerebellin-1Increased Spontaneous Otoacoustic Emissions in Mice with a Detached Tectorial Membrane.A novel mutation in the TECTA gene in a Chinese family with autosomal dominant nonsyndromic hearing loss.Prestin regulation and function in residual outer hair cells after noise-induced hearing loss.Molecular biology of hearing.Continued expression of GATA3 is necessary for cochlear neurosensory developmentDFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairmentGenetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion.
P2860

Characterization of a spontaneous, recessive, missense mutation arising in the Tecta gene.

Item
http://www.wikidata.org/entity/Q36824671
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Characterization of a spontane ...... ion arising in the Tecta gene.
@en
type
label
Characterization of a spontane ...... ion arising in the Tecta gene.
@en
prefLabel
Characterization of a spontane ...... ion arising in the Tecta gene.
@en
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P433
P478
P577
P5875
P698
P932
P356
P1433
P1476
Characterization of a spontane ...... ion arising in the Tecta gene.
@en
P2093
P2860
P2888
P304
P31
P356
P433
P478
P577
P5875
P698
P932