HAL (France)open access
Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss‐of‐function variants
BAZ2B, Autism spectrum disorder, Developmental delay, Intellectual disability, Neurodevelopmental disorder, 0, Genetic syndrome
This document is indexed with metadata only — full text is not available in the archive for this record.
Open the official source ↗
Record · ID 291663
Retrieved via
Conceptio — every document is proof-bundled with source, license, and retrieval metadata.