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.
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ABSTRACT:
SUBMITTER: Zhou C
PROVIDER: S-EPMC10476734 | biostudies-literature | 2023 Sep
REPOSITORIES: biostudies-literature
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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.
Zhou Cong C Wei Xing X Xiao Yuanyuan Y Liu Shanling S Wang Jing J
Chinese medical journal 20230905 17
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