Hearing Dysfunction in Xpa-Deficient Mice

Xeroderma pigmentosum (XP) is a rare recessive heredity disease caused by DNA repair impairment characterized by photosensitivity and neurologic symptoms in half of the cases. There are eight subtypes of XP: XP-A–XP-G and XP variant. Among eight subtypes, XP complementation group A (XP-A) display th...

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Detalles Bibliográficos
Autores principales: Shinomiya, Hitomi, Yamashita, Daisuke, Fujita, Takeshi, Nakano, Eiji, Inokuchi, Go, Hasegawa, Shingo, Otsuki, Naoki, Nishigori, Chikako, Nibu, Ken-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301083/
https://www.ncbi.nlm.nih.gov/pubmed/28239347
http://dx.doi.org/10.3389/fnagi.2017.00019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301083/
https://www.ncbi.nlm.nih.gov/pubmed/28239347
http://dx.doi.org/10.3389/fnagi.2017.00019

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