Global Variome shared LOVD

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Phenotype #0000034356 Individual ID 00046988 Associated disease NESCAVS Phenotype details Developmental delay, cerebellar atrophy, lower limb spasticity, and visual disturbance Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Hirotomo Saitsu Database submission license No license selected Created by Hirotomo Saitsu Date created 2015-08-04 12:12:50 +02:00 (CEST) Date last edited 2015-09-06 22:19:21 +02:00 (CEST)

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