Publications by authors named "Lingping Lu"

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An intronic mutation c.6430-3C>G in the F8 gene causes splicing efficiency and premature termination in hemophilia A.
Zunjing Xia, Jie Lin, Lingping Lu, Chol Kim, Ping Yu

Blood Coagul Fibrinolysis· June 2018

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A de novo mosaic mutation of PHEX in a boy with hypophosphatemic rickets.
Chen Weng, Jiao Chen, Li Sun, Zhong-Wei Zhou, Xue Feng, Ling-Ping Lu

J Hum Genet· March 2016

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The R900S mutation in CACNA1S associated with hypokalemic periodic paralysis.
Qing Ke, Fangping He, Lingping Lu, Ping Yu, Yajian Jiang

Neuromuscul Disord· December 2015

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A large deletion/insertion-induced frameshift mutation of the androgen receptor gene in a family with a familial complete androgen insensitivity syndrome.
Peikuan Cong, Yinghui Ye, Yue Wang, Lingping Lu, Jing Yong

Gene· June 2012

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