Expanding the neurodevelopmental phenotype associated with HK1 de novo heterozygous missense variants
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
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1. Clinical, Neuroimaging, and Metabolic Footprint of the Neurodevelopmental Disorder Caused by Monoallelic HK1 Variants;Neurology Genetics;2024-04
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