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Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder

PaperCitations, authors & open-access status

Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 25 citations, 2022 year and bronze oa status.

25
Citations
2022
Year
bronze
OA Status

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