Wang Q - Search Results

1

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.

Wang Q, Liu M, Xu C, Tang Z, Liao Y, Du R, Li W, Wu X, Wang X, Liu P, Zhang X, Zhu J, Ren X, Ke T, Wang Q, Yang J. Wang Q, et al. Among authors: wang x. J Mol Med (Berl). 2005 Mar;83(3):203-8. doi: 10.1007/s00109-005-0638-4. Epub 2005 Feb 22. J Mol Med (Berl). 2005. PMID: 15726306 Free PMC article.

2

[Mutation of Thr704Met in SCN 4A causes normoKPP in a Chinese family].

Ren X, Bu BT, Yao Q, Qiu X, Liu JY, Wang Q, Liu MG. Ren X, et al. Among authors: wang q. Yi Chuan. 2006 Aug;28(8):923-6. Yi Chuan. 2006. PMID: 16870577 Chinese.

3

Mutation p.Arg954Trp of KIF21A causes congenital fibrosis of the extraocular muscles in a Chinese family.

Zhang XQ, Peng JH, Tang ZH, Xu CQ, Zhou X, Gong SX, Liu JY, Wang Q, Liu MG. Zhang XQ, et al. Among authors: wang q. Yi Chuan Xue Bao. 2006 Aug;33(8):685-91. doi: 10.1016/S0379-4172(06)60100-5. Yi Chuan Xue Bao. 2006. PMID: 16939002

4

Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family.

Liu P, Li H, Ren X, Mao H, Zhu Q, Zhu Z, Yang R, Yuan W, Liu J, Wang Q, Liu M. Liu P, et al. Among authors: wang q. J Genet Genomics. 2008 Sep;35(9):553-8. doi: 10.1016/S1673-8527(08)60075-2. J Genet Genomics. 2008. PMID: 18804074

5

[A novel COL4A5 splicing mutation causing Alport syndrome in a Chinese family].

Tang Z, Dai Y, Wan Z, Zhan T, Tan J, Ren X, Liu J, Wang Q, Liu M. Tang Z, et al. Among authors: wang q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):649-52. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065523 Chinese.

6

Mutation c.359_363delGTATTinsATAC in the COL4A5 causes Alport syndrome in a Chinese family.

Wang Q, Liu F, Xing Y, Wei X, Li H, Zhang S, Liu J, Wang Q, Tang Z, Liu M. Wang Q, et al. Gene. 2013 Jan 10;512(2):482-5. doi: 10.1016/j.gene.2012.10.014. Epub 2012 Oct 18. Gene. 2013. PMID: 23085274 Clinical Trial.

7

Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects.

Tang ZH, Xia L, Chang W, Li H, Shen F, Liu JY, Wang Q, Liu MG. Tang ZH, et al. Among authors: wang q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):134-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16604480

8

The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family.

Ke T, Nie SW, Yang QB, Liu JP, Zhou LN, Ren X, Liu JY, Wang Q, Liu MG. Ke T, et al. Among authors: wang q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Oct;23(5):481-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 17029191

9

[Genetic analysis of GJB2 in a Chinese family with nonsyndromic hearing impairment].

Zhu QH, Li H, Liu P, Zhu ZF, Wang X, Yuan WL, Liu JY, Mao HY, Wang Q, Liu MG. Zhu QH, et al. Among authors: wang x, wang q. Yi Chuan. 2007 Feb;29(2):172-6. doi: 10.1360/yc-007-0172. Yi Chuan. 2007. PMID: 17369171 Chinese.

10

Ser217Cys mutation in the Ig II domain of FGFR3 in a Chinese family with autosomal dominant achondroplasia.

Zhang SR, Zhou XQ, Ren X, Wang TT, Yuan MX, Wang Q, Liu JY, Liu MG. Zhang SR, et al. Among authors: wang tt, wang q. Chin Med J (Engl). 2007 Jun 5;120(11):1017-9. Chin Med J (Engl). 2007. PMID: 17624273 No abstract available.

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