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The nob2 mouse, a null mutation in Cacna1f: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses

Glutamate release from photoreceptor terminals is controlled by voltage-dependent calcium channels (VDCCs). In humans, mutations in the Cacna1f gene, encoding the α(1F) subunit of VDCCs, underlie the incomplete form of X-linked congenital stationary night blindness (CSNB2). These mutations impair sy...

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التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	CHANG, BO, HECKENLIVELY, JOHN R., BAYLEY, PHILIPPA R., BRECHA, NICHOLAS C., DAVISSON, MURIEL T., HAWES, NORM L., HIRANO, ARLENE A., HURD, RONALD E., IKEDA, AKIHIRO, JOHNSON, BRITT A., MCCALL, MAUREEN A., MORGANS, CATHERINE W., NUSINOWITZ, STEVE, PEACHEY, NEAL S., RICE, DENNIS S., VESSEY, KIRSTAN A., GREGG, RONALD G.
التنسيق:	Artigo
اللغة:	Inglês
منشور في:	2006
الموضوعات:	Article
الوصول للمادة أونلاين:	https://ncbi.nlm.nih.gov/pmc/articles/PMC2831086/ https://ncbi.nlm.nih.gov/pubmed/16597347 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S095252380623102X
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The nob2 mouse, a null mutation in Cacna1f: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses

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