Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy

Méjécase, C; Laurent-Coriat, C; Mayer, C; Poch, O; Mohand-Saïd, S; Prévot, C; Antonio, A; ... Zeitz, C; + view all Méjécase, C; Laurent-Coriat, C; Mayer, C; Poch, O; Mohand-Saïd, S; Prévot, C; Antonio, A; Boyard, F; Condroyer, C; Michiels, C; Blanchard, S; Letexier, M; Saraiva, J-P; Sahel, J-A; Audo, I; Zeitz, C; - view fewer (2016) Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy. PLoS One , 11 (12) , Article e0168271. 10.1371/journal.pone.0168271 . Green open access

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