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

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Publication | Open Access

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

DOI Full Paper Access

22

Citations

26

References

2022

Year

Sébastien Küry, Frédéric Ebstein, Alice Mollé, Thomas Besnard, Ming-Kang Lee, Virginie Vignard, Tiphaine Héry, Mathilde Nizon, Grazia M.S. Mancini, Jacques C. Giltay,

The American Journal of Human Genetics

Developmental BiologyMolecular NeuroscienceSyndromic Neurodevelopmental DisorderBrain DevelopmentGenetic DisorderGeneticsBrca1-associated Protein 1NeuroscienceDisease Gene IdentificationMedicineSocial SciencesNeurogenetics

References

	Year	Citations

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