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

Fuente: PubMed

Saved in:

Bibliographic Details
Main Authors:	Pan, Yang, Iejima, Daisuke, Yoshitake, Kazutoshi, Tsunoda, Kazushige, Iwata, Takeshi
Format:	Artículo científico
Language:	en
Published:	HGG advances 2025
Subjects:	Humans Macular Degeneration Male Female Eye Proteins Pedigree Mutation Middle Aged Adult Microtubule-Associated Proteins Exome Sequencing Phenotype Electroretinography
Online Access:	Acceder al recurso
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Description not available.

Similar Items