Wang N - Search Results

1

Cryptic exon activation causes dystrophinopathy in two Chinese families.

Jin M, Li JJ, Xu GR, Wang N, Wang ZQ. Jin M, et al. Among authors: wang n, wang zq. Eur J Hum Genet. 2020 Jul;28(7):947-955. doi: 10.1038/s41431-020-0578-z. Epub 2020 Feb 11. Eur J Hum Genet. 2020. PMID: 32047267 Free PMC article.

2

[Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy].

Wang N, Wu ZY, Wang CD, Wang ZQ, Lin MT, Fang L, Murong SX. Wang N, et al. Among authors: wang cd, wang zq. Zhonghua Yi Xue Za Zhi. 2003 Apr 25;83(8):650-3. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12887821 Chinese.

3

FSHD in Chinese population: characteristics of translocation and genotype-phenotype correlation.

Wu ZY, Wang ZQ, Murong SX, Wang N. Wu ZY, et al. Among authors: wang n, wang zq. Neurology. 2004 Aug 10;63(3):581-3. doi: 10.1212/01.wnl.0000133210.93075.81. Neurology. 2004. PMID: 15304602

4

[Study on EcoR I fragment polymorphism of the subtelomeric domains within 4q35 and 10q26 with pulsed field gel electrophoresis in the Chinese population].

Wu ZY, Wang ZQ, Wang N, Lin MT, Murong SX. Wu ZY, et al. Among authors: wang n, wang zq. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):552-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583980 Chinese.

5

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

6

New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients.

Lin F, Wang ZQ, Lin MT, Murong SX, Wang N. Lin F, et al. Among authors: wang n, wang zq. Chin Med J (Engl). 2015 Jul 5;128(13):1707-13. doi: 10.4103/0366-6999.159336. Chin Med J (Engl). 2015. PMID: 26112708 Free PMC article.

7

A Historical Cohort Study on the Efficacy of Glucocorticoids and Riboflavin Among Patients with Late-onset Multiple Acyl-CoA Dehydrogenase Deficiency.

Liu XY, Wang ZQ, Wang DN, Lin MT, Wang N. Liu XY, et al. Among authors: wang n, wang zq, wang dn. Chin Med J (Engl). 2016 Jan 20;129(2):142-6. doi: 10.4103/0366-6999.173438. Chin Med J (Engl). 2016. PMID: 26830983 Free PMC article.

8

Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.

Fu HX, Liu XY, Wang ZQ, Jin M, Wang DN, He JJ, Lin MT, Wang N. Fu HX, et al. Among authors: wang n, wang zq, wang dn. Neurol Sci. 2016 Jul;37(7):1099-105. doi: 10.1007/s10072-016-2549-2. Epub 2016 Mar 21. Neurol Sci. 2016. PMID: 27000805

9

Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations.

Liu XY, Jin M, Wang ZQ, Wang DN, He JJ, Lin MT, Fu HX, Wang N. Liu XY, et al. Among authors: wang n, wang zq, wang dn. Chin Med J (Engl). 2016 Jun 20;129(12):1425-31. doi: 10.4103/0366-6999.183423. Chin Med J (Engl). 2016. PMID: 27270537 Free PMC article.

10

Modeling the phenotype of spinal muscular atrophy by the direct conversion of human fibroblasts to motor neurons.

Zhang QJ, Li JJ, Lin X, Lu YQ, Guo XX, Dong EL, Zhao M, He J, Wang N, Chen WJ. Zhang QJ, et al. Among authors: wang n. Oncotarget. 2017 Feb 14;8(7):10945-10953. doi: 10.18632/oncotarget.14641. Oncotarget. 2017. PMID: 28099929 Free PMC article.

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