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Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A.
Wang ZQ, Chen XJ, Murong SX, Wang N, Wu ZY. Wang ZQ, et al. Among authors: murong sx. J Mol Med (Berl). 2011 Jun;89(6):569-76. doi: 10.1007/s00109-011-0725-7. Epub 2011 Feb 24. J Mol Med (Berl). 2011. PMID: 21347544
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: murong sx. 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
Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.
Wu ZY, Zhao GX, Chen WJ, Wang N, Wan B, Lin MT, Murong SX, Yu L. Wu ZY, et al. J Mol Med (Berl). 2006 May;84(5):438-42. doi: 10.1007/s00109-005-0036-y. Epub 2006 Jan 28. J Mol Med (Berl). 2006. PMID: 16649058
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
Chen WJ, Lin Y, Xiong ZQ, Wei W, Ni W, Tan GH, Guo SL, He J, Chen YF, Zhang QJ, Li HF, Lin Y, Murong SX, Xu J, Wang N, Wu ZY. Chen WJ, et al. Among authors: murong sx. Nat Genet. 2011 Nov 20;43(12):1252-5. doi: 10.1038/ng.1008. Nat Genet. 2011. PMID: 22101681
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: murong sx. 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.
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: murong sx. Gene. 2013 Apr 15;518(2):325-9. doi: 10.1016/j.gene.2012.12.109. Epub 2013 Jan 23. Gene. 2013. PMID: 23352792
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: murong sx. Gene. 2013 Oct 15;529(1):159-62. doi: 10.1016/j.gene.2013.07.071. Epub 2013 Aug 11. Gene. 2013. PMID: 23939468
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