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Levin A 1

Showing records 1 to 1 | Display all abstracts from Levin A

95528 CNGB1-related rod-cone dystrophy: A mutation review and update
Nassisi M; Smirnov VM; Solis Hernandez C; Mohand-Saïd S; Condroyer C; Antonio A; Kühlewein L; Kempf M; Kohl S; Wissinger B; Nasser F; Ragi SD; Wang NK; Sparrow JR; Greenstein VC; Michalakis S; Mahroo OA; Ba-Abbad R; Michaelides M; Webster AR; Degli Esposti S; Saffren B; Capasso J; Levin A; Hauswirth WW; Dhaenens CM; Defoort-Dhellemmes S; Tsang SH; Zrenner E; Sahel JA; Petersen-Jones SM; Zeitz C; Audo I
Human Mutation 2021; 42: 641-666

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