GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.

N.S. Peachey; T.A. Ray; R.J. Florijn; L.B. Rowe; T. Sjoerdsma; S. Contreras-Alcantara; K. Baba; G. Tosini; N. Pozdeyev; P.M. Iuvone; P. Bojang; J.N. Pearring; H.J. Simonsz; M.M. Van Genderen; D.G. Birch; W.I. Traboulsi; A. Dorfman; I. Lopez; H. Ren; A.F. Goldberg; P.M. Nishina; P. Lachapelle; M.A. McCall; R.K. Koenekoop; A.A.B. Bergen; M. Kamermans; R.G. Gregg

doi:10.1016/j.ajhg.2011.12.006

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.

N.S. Peachey, T.A. Ray, R.J. Florijn, L.B. Rowe, T. Sjoerdsma, S. Contreras-Alcantara, K. Baba, G. Tosini, N. Pozdeyev, P.M. Iuvone, P. Bojang, J.N. Pearring, H.J. Simonsz, M.M. Van Genderen, D.G. Birch, W.I. Traboulsi, A. Dorfman, I. Lopez, H. Ren, A.F. GoldbergP.M. Nishina, P. Lachapelle, M.A. McCall, R.K. Koenekoop, A.A.B. Bergen, M. Kamermans, R.G. Gregg

Netherlands Institute for Neuroscience (NIN)

Research output: Contribution to journal/periodical › Article › Scientific › peer-review

126 Citations (Scopus)

Original language	English
Pages (from-to)	331-339
Journal	American Journal of Human Genetics
Volume	90
DOIs	https://doi.org/10.1016/j.ajhg.2011.12.006
Publication status	Published - 2012

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10.1016/j.ajhg.2011.12.006

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Peachey, N. S., Ray, T. A., Florijn, R. J., Rowe, L. B., Sjoerdsma, T., Contreras-Alcantara, S., Baba, K., Tosini, G., Pozdeyev, N., Iuvone, P. M., Bojang, P., Pearring, J. N., Simonsz, H. J., Van Genderen, M. M., Birch, D. G., Traboulsi, W. I., Dorfman, A., Lopez, I., Ren, H., ... Gregg, R. G. (2012). GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness. American Journal of Human Genetics, 90, 331-339. https://doi.org/10.1016/j.ajhg.2011.12.006

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title = "GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.",

author = "N.S. Peachey and T.A. Ray and R.J. Florijn and L.B. Rowe and T. Sjoerdsma and S. Contreras-Alcantara and K. Baba and G. Tosini and N. Pozdeyev and P.M. Iuvone and P. Bojang and J.N. Pearring and H.J. Simonsz and {Van Genderen}, M.M. and D.G. Birch and W.I. Traboulsi and A. Dorfman and I. Lopez and H. Ren and A.F. Goldberg and P.M. Nishina and P. Lachapelle and M.A. McCall and R.K. Koenekoop and A.A.B. Bergen and M. Kamermans and R.G. Gregg",

note = "Reporting year: 2012",

year = "2012",

doi = "10.1016/j.ajhg.2011.12.006",

language = "English",

volume = "90",

pages = "331--339",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

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Peachey, NS, Ray, TA, Florijn, RJ, Rowe, LB, Sjoerdsma, T, Contreras-Alcantara, S, Baba, K, Tosini, G, Pozdeyev, N, Iuvone, PM, Bojang, P, Pearring, JN, Simonsz, HJ, Van Genderen, MM, Birch, DG, Traboulsi, WI, Dorfman, A, Lopez, I, Ren, H, Goldberg, AF, Nishina, PM, Lachapelle, P, McCall, MA, Koenekoop, RK, Bergen, AAB , Kamermans, M & Gregg, RG 2012, 'GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.', American Journal of Human Genetics, vol. 90, pp. 331-339. https://doi.org/10.1016/j.ajhg.2011.12.006

TY - JOUR

T1 - GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.

AU - Peachey, N.S.

AU - Ray, T.A.

AU - Florijn, R.J.

AU - Rowe, L.B.

AU - Sjoerdsma, T.

AU - Contreras-Alcantara, S.

AU - Baba, K.

AU - Tosini, G.

AU - Pozdeyev, N.

AU - Iuvone, P.M.

AU - Bojang, P.

AU - Pearring, J.N.

AU - Simonsz, H.J.

AU - Van Genderen, M.M.

AU - Birch, D.G.

AU - Traboulsi, W.I.

AU - Dorfman, A.

AU - Lopez, I.

AU - Ren, H.

AU - Goldberg, A.F.

AU - Nishina, P.M.

AU - Lachapelle, P.

AU - McCall, M.A.

AU - Koenekoop, R.K.

AU - Bergen, A.A.B.

AU - Kamermans, M.

AU - Gregg, R.G.

N1 - Reporting year: 2012

PY - 2012

Y1 - 2012

U2 - 10.1016/j.ajhg.2011.12.006

DO - 10.1016/j.ajhg.2011.12.006

M3 - Article

SN - 0002-9297

VL - 90

SP - 331

EP - 339

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

ER -