Associated Papers
Mutation analysis of seven SLC family transporters for early-onset Parkinson's disease in Chinese population.
Li C et al.
Neurobiology of Aging, 2021
Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella.
Shen Y et al.
Nature Communications, 2019
30683861 (PubMed )
Supplement: 41467_2018_8182_MOESM10_ESM.xls › PA
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