Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses

BACKGROUND: Mutations in the Otopetrin 1 gene (Otop1) in mice and fish produce an unusual bilateral vestibular pathology that involves the absence of otoconia without hearing impairment. The encoded protein, Otop1, is the only functionally characterized member of the Otopetrin Domain Protein (ODP) f...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Hurle, Belen, Marques-Bonet, Tomas, Antonacci, Francesca, Hughes, Inna, Ryan, Joseph F, Eichler, Evan E, Ornitz, David M, Green, Eric D
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2011
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3038909/
https://ncbi.nlm.nih.gov/pubmed/21261979
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2148-11-23
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