Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis (Q24678616)
scientific article
Language:
(P31) (Q13442814)
(Q2782326)
(P50) (Q28039310)
(Q22669719)
(Q86185304)
(Q92051039)
(Q89601885)
(Q92869049)
(Q114716878)
(Q59554006)
(Q114316329)
(Q87773819)
(P304) 556-61
(P407) (Q1860)
(P433) 3
(P478) 79
(P577) +2006-09-00T00:00:00Z
(P921) (Q727096)
(Q1811132)
(P1433) (Q4744249)
(P1476) "Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis" (language: en)
(P2093) Suzanne Yzer
Irma Lopez
Krysta E J Voesenek
Klaus Rohrschneider
(P2860) (Q24336477)
(Q24671808)
(Q24642869)
(Q24540237)
(Q28239026)
(Q28299434)
(Q28250847)
(Q28141825)
(Q28262021)
(Q29618621)
(Q29618620)
(Q30994046)
(Q34334012)
(Q34641603)
(Q46338894)
(Q46670192)
(Q73087273)
other details
description scientific article

External Links