Global Variome shared LOVD

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Phenotype #0000350744 Individual ID 00465208 Associated disease - Phenotype details see paper; ..., night blindness, reduced visual acuity; onset early childhood; fundus retinitis pigmentosa Diagnosis/Initial non-syndromic X-linked retinal degeneration Inheritance Familial, X-linked recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset night blindness, reduced visual acuity Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2025-04-14 16:53:34 +02:00 (CEST) Date last edited 2025-04-14 17:45:09 +02:00 (CEST)

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