Global Variome shared LOVD

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Phenotype #0000090376 Individual ID 00114911 Associated disease DEE2 Inheritance Unknown Diagnosis/Initial - Age/Examination - Diagnosis/Definite - Age/Diagnosis - Age/Onset - Phenotype/Onset - Phenotype details Rett syndrome (variant), infantile seizures, acquired microcephaly, hand apraxia, generalized hypotonia, stereotypic hand motions; EIEE2 Protein - Owner name Emmelien Aten Database submission license No license selected Created by Emmelien Aten Date created 2010-10-24 14:36:15 +02:00 (CEST) Date last edited N/A

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