Li Li
4PUBLICATIONS
1CO-AUTHORS
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Publications (4)
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|Jan 19, 2024
Phenotypes of a toddler with hereditary sensory and autonomic neuropathy type IV: comparing with normal: A case report.Qinghua Xu, Yanchun Wang, Yuantao Zhou
|Oct 18, 2022
Potential pathogenic mechanism of type 1 X-linked lymphoproliferative syndrome caused by a mutation of SH2D1A gene in an infant: A case report.Yanchun Wang, Yan Wang, Weimin Lu
|Jul 08, 2022
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.Yangfang Li, Yu Zhang, Gengpan Jiang
|Apr 21, 2021
Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports.Haifeng Liu, Yanchun Wang, Yangfang Li
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