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Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis
scientific article
Author/s
author: Thomas Meitinger, Han G. Brunner, Robert Koenekoop, Frans P M Cremers, Anneke den Hollander, Carel B Hoyng, L Ingeborgh van den Born, Marijke I Zonneveld, Tim M Strom, Maarten Arends
Work details
Publication date
September 2006
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Language
English
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