Global Variome shared LOVD

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Phenotype #0000186447 Individual ID 00246590 Associated disease CSNB Phenotype details see paper; ..., lifelong night-blindness, significant pigmentary disturbance, constriction of visual fields (retinitis pigmentosa) Diagnosis/Initial night blindness Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2019-07-14 12:52:49 +02:00 (CEST) Date last edited N/A

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