S-EPMC10476734 - Novel compound heterozygous variants in lectin mannose-binding 2-like gene identified in a Chinese autosomal recessive mental retardation-52 (MRT52) patient with phenotype expansion. - OmicsDI

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Novel compound heterozygous variants in lectin mannose-binding 2-like gene identified in a Chinese autosomal recessive mental retardation-52 (MRT52) patient with phenotype expansion.

ABSTRACT:

SUBMITTER: Zhou C

PROVIDER: S-EPMC10476734 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature