A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction
Autor: | Rh, Henderson, Ka, Williamson, Js, Kennedy, Ar, Webster, Ge, Holder, Anthony Robson, Dr, Fitzpatrick, van Heyningen V, At, Moore |
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Zdroj: | Europe PubMed Central |
Databáze: | OpenAIRE |
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