Associated Papers
Digenic CHD7 and SMCHD1 inheritance Unveils phenotypic variability in a family mainly presenting with hypogonadotropic hypogonadism.
Wang T et al.
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Rare variant analysis of PLXNA1 in Parkinson's disease in the Chinese population.
Li C et al.
Genes & Diseases, 2023
37397528 (PubMed )
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