New Insights on the Regulatory Gene Network Disturbed in Central Areolar Choroidal Dystrophy—Beyond Classical Gene Candidates

Central areolar choroidal dystrophy (CACD) is a rare hereditary disease that mainly affects the macula, resulting in progressive and usually profound visual loss. Being part of congenital retinal dystrophies, it may have an autosomal dominant or recessive inheritance and, until now, has no effective...

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Detalhes bibliográficos
Main Authors: João Paulo Kazmierczak de Camargo, Giovanna Nazaré de Barros Prezia, Naoye Shiokawa, Mario Teruo Sato, Roberto Rosati, Angelica Beate Winter Boldt
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2022-05-01
Colecção:Frontiers in Genetics
Assuntos:
macular disease
CACD
central areolar choroidal distrophy
PRPH2
GUCA1A
GUCY2D
Acesso em linha:https://www.frontiersin.org/articles/10.3389/fgene.2022.886461/full
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