Publications
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Filters: Keyword is Mutation, Missense and Author is Raymond, F Lucy [Clear All Filters]
SYT1-associated neurodevelopmental disorder: a case series. Brain. 2018 ;141(9):2576-2591.
. Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa. Am J Hum Genet. 2016 ;99(6):1305-1315.
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