Global Variome shared LOVD

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Phenotype #0000245955 Individual ID 00327727 Associated disease - Phenotype details see paper; ..., congenital stationary night blindness (HP:0007642) Diagnosis/Initial congenital stationary night blindness Inheritance Familial, X-linked Diagnosis/Definite CSNB2A Age/Examination 07y (7 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Christina Zeitz Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-01-26 18:51:45 +01:00 (CET) Date last edited 2021-01-28 09:18:24 +01:00 (CET)

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