Zobrazeno 1 - 10 of 35 pro vyhledávání: '"M, Delle Fave"'
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Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in TRPM1
Autor: Christel Condroyer, M Cordonnier, Christina Zeitz, L Vallee, Irina Balikova, M Delle Fave
Publikováno v: Ophthalmic Genetics. 42:296-299
The complete form of congenital stationary night blindness (cCSNB) represents a non-progressive retinal disorder characterized by night vision problems and often congenital nystagmus, reduced vision, high myopia, strabismus and normal fundus appearan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::94892fe4498f50c3d8720f365f28b794
https://doi.org/10.1080/13816810.2021.1897846
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9
Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in
Autor: M, Delle Fave, M, Cordonnier, L, Vallee, C, Condroyer, C, Zeitz, I, Balikova
Publikováno v: Ophthalmic genetics. 42(3)
The complete form of congenital stationary night blindness (cCSNB) represents a non-progressive retinal disorder characterized by night vision problems and often congenital nystagmus, reduced vision, high myopia, strabismus and normal fundus appearan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9a1137e69d56e93c00f9ffe325756f62
https://pubmed.ncbi.nlm.nih.gov/33691579
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Plný text Recenzováno Digitální knihovna AV ČR
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