학술논문

Rare mosaic variant of GJA1 in a patient with a neurodevelopmental disorder.
Document Type
Article
Source
Human Genome Variation; 1/15/2024, Vol. 11 Issue 1, p1-4, 4p
Subject
NEURAL development
DYSPLASIA
SHORT stature
DENTAL enamel
HEARING disorders
MYELINATION
Language
ISSN
2054345X
Abstract
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