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Affymetrix SNP array data for an INAD patient

ABSTRACT: Infantile neuroaxonal dystrophy (INAD) is an ultra-rare early-onset autosomal recessive neurodegenerative disorder due to PLA2G6 variants. Copy number analysis of SNP arrays was performed on one INAD patient sample.

ORGANISM(S): Homo sapiens

PROVIDER: GSE233748 | GEO | 2023/05/31

REPOSITORIES: GEO

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