Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.

Authors :: Thiadens, A.A.H.J.
Den Hollander, A.I.
Roosing, S.
Nabuurs, S.B.
Zekveld-Vroon, R.C.
Collin, R.W.J.
De Baere, E.
Koenekoop, R.K.
Van Schooneveld, M.J.
Strom, T.M.
Van Lith-Verhoeven, J.J.C.
Lotery, A.J.
Van Moll-Ramirez, N.
Leroy, B.P.
Van den Born, L.I.
Hoyng, C.B.
Cremers, F.P.M.
Klaver, C.C.
Thiadens, A.A.H.J.
Den Hollander, A.I.
Roosing, S.
Nabuurs, S.B.
Zekveld-Vroon, R.C.
Collin, R.W.J.
De Baere, E.
Koenekoop, R.K.
Van Schooneveld, M.J.
Strom, T.M.
Van Lith-Verhoeven, J.J.C.
Lotery, A.J.
Van Moll-Ramirez, N.
Leroy, B.P.
Van den Born, L.I.
Hoyng, C.B.
Cremers, F.P.M.
Klaver, C.C.
Source :: American Journal of Human Genetics vol.85 (2009) p.240-247 [ISSN 0002-9297]
Publication Year :: 2009

Database :: OAIster
Journal :: American Journal of Human Genetics vol.85 (2009) p.240-247 [ISSN 0002-9297]
Notes :: DOI: 10.1016/j.ajhg.2009.06.016, American Journal of Human Genetics vol.85 (2009) p.240-247 [ISSN 0002-9297], English
Publication Type :: Electronic Resource
Accession number :: edsoai.on1367004177
Document Type :: Electronic Resource

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