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Article

Studying ultra-rare variants in STX1A uncovers a novel neurodevelopmental disorder.

European journal of human genetics : EJHG - 1 Sept 2023

Villavicencio Gonzalez Esmeralda, Dhindsa Ryan S

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Identifiers

PMID: 37029317
DOI: 10.1038/s41431-023-01348-2
PMCID: PMC10474260

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Studying ultra-rare variants in STX1A uncovers a novel neurodevelopmental disorder.PMID 37029317Read ↗

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