Global Variome shared LOVD

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Phenotype #0000038135 Individual ID 00051532 Associated disease BCS2 Phenotype details see paper, brittel cornea syndrome, ... Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Shazia Micheal Database submission license No license selected Created by Johan den Dunnen Date created 2015-10-02 21:56:52 +02:00 (CEST) Date last edited 2017-11-29 08:07:01 +01:00 (CET)

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