Global Variome shared LOVD

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Phenotype #0000277268 Individual ID 00383483 Associated disease CLN Phenotype details retinal dysfunction on ERG, VEP results: atypical Diagnosis/Initial lipofuscinosis, ceroid, neuronal, type 7 (CLN7) Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-09-29 11:58:04 +02:00 (CEST) Date last edited N/A

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