Wang N - Search Results

1

ATP1A1 mutations cause intermediate Charcot-Marie-Tooth disease.

He J, Guo L, Lin S, Chen W, Xu G, Cai B, Xu L, Hong J, Qiu L, Wang N, Chen W. He J, et al. Among authors: wang n. Hum Mutat. 2019 Dec;40(12):2334-2343. doi: 10.1002/humu.23886. Epub 2019 Aug 23. Hum Mutat. 2019. PMID: 31373411

2

Rapid diagnosis of spinal muscular atrophy using denaturing high-performance liquid chromatography.

Chen WJ, Wu ZY, Wang N, Lin MT, Mu-Rong SX. Chen WJ, et al. Among authors: wang n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):291-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952118

3

Modification of phenotype by SMN2 copy numbers in two Chinese families with SMN1 deletion in two continuous generations.

Chen WJ, He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N. Chen WJ, et al. Among authors: wang n. Clin Chim Acta. 2012 Nov 20;413(23-24):1855-60. doi: 10.1016/j.cca.2012.07.020. Epub 2012 Aug 4. Clin Chim Acta. 2012. PMID: 22884440

4

Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.

He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N, Chen WJ. He J, et al. Among authors: wang n. Gene. 2013 Apr 15;518(2):325-9. doi: 10.1016/j.gene.2012.12.109. Epub 2013 Jan 23. Gene. 2013. PMID: 23352792

5

Noninvasive urine-derived cell lines derived from neurological genetic patients.

Zhang QJ, He J, Ni W, Lin X, Yao XP, Lin MT, Murong SX, Wang N, Chen WJ. Zhang QJ, et al. Among authors: wang n. Neuroreport. 2013 Mar 6;24(4):161-6. doi: 10.1097/WNR.0b013e32835e2e44. Neuroreport. 2013. PMID: 23358449

6

PRRT2 mutation correlated with phenotype of paroxysmal kinesigenic dyskinesia and drug response.

Li HF, Chen WJ, Ni W, Wang KY, Liu GL, Wang N, Xiong ZQ, Xu J, Wu ZY. Li HF, et al. Among authors: wang ky, wang n. Neurology. 2013 Apr 16;80(16):1534-5. doi: 10.1212/WNL.0b013e31828cf7e1. Epub 2013 Mar 27. Neurology. 2013. PMID: 23535490 No abstract available.

7

Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing.

Chen WJ, Lin QF, Zhang QJ, He J, Liu XY, Lin MT, Murong SX, Liou CW, Wang N. Chen WJ, et al. Among authors: wang n. Clin Chim Acta. 2013 Aug 23;423:35-8. doi: 10.1016/j.cca.2013.04.006. Epub 2013 Apr 13. Clin Chim Acta. 2013. PMID: 23588064

8

Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China.

Cai J, Lin Y, Chen W, Lin Q, Cai B, Wang N, Zheng W. Cai J, et al. Among authors: wang n. Neurol Sci. 2013 Nov;34(11):2001-6. doi: 10.1007/s10072-013-1436-3. Epub 2013 Apr 30. Neurol Sci. 2013. PMID: 23624603

9

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.

Chen WJ, Yao XP, Zhang QJ, Ni W, He J, Li HF, Liu XY, Zhao GX, Murong SX, Wang N, Wu ZY. Chen WJ, et al. Among authors: wang n. Gene. 2013 Oct 15;529(1):159-62. doi: 10.1016/j.gene.2013.07.071. Epub 2013 Aug 11. Gene. 2013. PMID: 23939468

10

Variations of IGHMBP2 gene was not the major cause of Han Chinese patients with non-5q-spinal muscular atrophies.

Lin X, Zhang QJ, He J, Lin MT, Murong SX, Wang N, Chen WJ. Lin X, et al. Among authors: wang n. J Child Neurol. 2014 Aug;29(8):NP35-9. doi: 10.1177/0883073813497827. Epub 2013 Sep 9. J Child Neurol. 2014. PMID: 24022109

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