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WGA Rescources

Kim AH 15

Showing records 1 to 15 | Display all abstracts from Kim AH

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