Associated Papers
Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia.
Vaz FM et al.
Brain : a Journal of Neurology, 2019
31637422 (PubMed )
Supplement: awz291_supplementary_data.zip › awz291-Suppl_data › Supplementary_Data2.pdf
[Correlation of the autophagosome gene ATG16L1 polymorphism and inflammatory bowel disease].
Zhi J et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University, 2008
[Relationship of collagen type I alpha 1 and alpha 2 gene polymorphisms with bone mineral density].
Li DF et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University, 2006
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