S-EPMC10689817 - Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome. - OmicsDI

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Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome.

ABSTRACT:

SUBMITTER: Kumps C

PROVIDER: S-EPMC10689817 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature