Buchumschlag

Clinical features and molecular mechanisms of RP1L1 variants causing occult macular dystrophy.

Fuente: PubMed

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Bibliographische Detailangaben
Hauptverfasser:	Pan, Yang, Iejima, Daisuke, Yoshitake, Kazutoshi, Tsunoda, Kazushige, Iwata, Takeshi
Format:	Artículo científico
Sprache:	en
Veröffentlicht:	HGG advances 2025
Schlagworte:	Humans Macular Degeneration Male Female Eye Proteins Pedigree Mutation Middle Aged Adult Microtubule-Associated Proteins Exome Sequencing Phenotype Electroretinography
Online-Zugang:	Acceder al recurso
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

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