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Case report: novel mutations of NDUFS6 and NHLRC2 genes potentially cause the quick postnatal death of a Chinese Hani minority neonate with mitochondrial complex I deficiency and FINCA syndrome.
Medicine (Baltimore). 2022 Jul 8;101(27):e29239. doi: 10.1097/MD.0000000000029239.
Medicine (Baltimore). 2022.
PMID: 35801790
Free PMC article.
Expression of vimentin and glial fibrillary acidic protein in central nervous system development of rats.
Luo H, Wu XQ, Zhao M, Wang Q, Jiang GP, Cai WJ, Luo MY.
Luo H, et al.
Asian Pac J Trop Med. 2017 Dec;10(12):1185-1189. doi: 10.1016/j.apjtm.2017.10.027. Epub 2017 Oct 28.
Asian Pac J Trop Med. 2017.
PMID: 29268976
Free article.
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