Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290
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Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290
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im September 2018 veröffentlichter wissenschaftlicher Artikel
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scientific article published on 01 September 2018
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name
Clinical Characterization of 6 ...... 991+1655A>G Mutation in CEP290
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type
label
Clinical Characterization of 6 ...... 991+1655A>G Mutation in CEP290
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prefLabel
Clinical Characterization of 6 ...... 991+1655A>G Mutation in CEP290
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P2093
P356
P1476
Clinical Characterization of 6 ...... 991+1655A>G Mutation in CEP290
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P2093
Alberta A H J Thiadens
Bart P Leroy
Birgit Lorenz
Carel B Hoyng
Caroline C W Klaver
Dyon Valkenburg
Hester Y Kroes
Jan-Willem R Pott
Julie de Zaeytijd
L Ingeborgh van den Born
P304
P356
10.1167/IOVS.18-24817
P577
2018-09-01T00:00:00Z