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WGA Rescources

Kolesnikova M 10

Showing records 1 to 10 | Display all abstracts from Kolesnikova M

106030 Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence
Kolesnikova M
Molecular genetics & genomic medicine 2022; 10: e2038
106109 A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
Kolesnikova M; Kolesnikova M
JCI insight 2022; 7:
106030 Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence
Kolesnikova M; Lima de Carvalho JR
Molecular genetics & genomic medicine 2022; 10: e2038
106109 A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
Oh JK; Wang J
JCI insight 2022; 7:
106030 Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence
Parmann R; Kim AH; Kim AH
Molecular genetics & genomic medicine 2022; 10: e2038
106109 A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
Lee W; Zernant J
JCI insight 2022; 7:
106030 Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence
Mahajan VB
Molecular genetics & genomic medicine 2022; 10: e2038
106109 A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
Su PY; Su PY
JCI insight 2022; 7:
106030 Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence
Tsang SH; Sparrow JR
Molecular genetics & genomic medicine 2022; 10: e2038
106109 A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
Kim AH; Kim AH; Jenny LA; Yang T; Allikmets R; Tsang SH
JCI insight 2022; 7:

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