Associated Papers
From Beginning to End: Expanding the SERINC3 Interactome Through an in silico Analysis.
Tu M et al.
Bioinformatics and Biology Insights, 2022
35494555 (PubMed )
Supplement: sj-xlsx-1-bbi-10.1177_11779322221092944.xlsx › Table_S6
A Gly684Ala substitution in the androgen receptor is the cause for azoospermia in a Chinese family with mild androgen insensitivity syndrome and normal hormone levels.
Yuan Y et al.
Frontiers in Genetics, 2022
36159980 (PubMed )
Supplement: Table1.XLSX › SNP
Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion.
Onat OE et al.
European Journal of Human Genetics : Ejhg, 2013
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