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jinqi, bai
(13 results)?
Familial study of spinal muscular atrophy carriers with SMN1 (2+0) genotype.
Yi Chuan. 2021 Feb 16;43(2):160-168. doi: 10.16288/j.yczz.20-319.
Yi Chuan. 2021.
PMID: 33724218
Correlation of PLS3 expression with disease severity in children with spinal muscular atrophy.
Yanyan C, Yujin Q, Jinli B, Yuwei J, Hong W, Fang S.
Yanyan C, et al. Among authors: jinli b.
J Hum Genet. 2014 Jan;59(1):24-7. doi: 10.1038/jhg.2013.111. Epub 2013 Oct 31.
J Hum Genet. 2014.
PMID: 24172247
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Subtle mutations in the SMN1 gene in Chinese patients with SMA: p.Arg288Met mutation causing SMN1 transcript exclusion of exon7.
Yu-Jin Q, Juan D, Er-zhen L, Jin-li B, Yu-wei J, Hong W, Fang S.
Yu-Jin Q, et al.
BMC Med Genet. 2012 Sep 20;13:86. doi: 10.1186/1471-2350-13-86.
BMC Med Genet. 2012.
PMID: 22994313
Free PMC article.
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