Literature DB >> 17026625

Large deletions of the MECP2 gene in Chinese patients with classical Rett syndrome.

H Pan, M-R Li, P Nelson, X-H Bao, X-R Wu, S Yu.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2006        PMID： 17026625     DOI： 10.1111/j.1399-0004.2006.00694.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


× No keyword cloud information.
  2 in total

Review 1.  CNV and nervous system diseases--what's new?

Authors:  W Gu; J R Lupski
Journal:  Cytogenet Genome Res       Date:  2009-03-11       Impact factor: 1.636

2.  NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation.

Authors:  Vincenzo A Gennarino; Callison E Alcott; Chun-An Chen; Arindam Chaudhury; Madelyn A Gillentine; Jill A Rosenfeld; Sumit Parikh; James W Wheless; Elizabeth R Roeder; Dafne D G Horovitz; Erin K Roney; Janice L Smith; Sau W Cheung; Wei Li; Joel R Neilson; Christian P Schaaf; Huda Y Zoghbi
Journal:  Elife       Date:  2015-08-27       Impact factor: 8.140
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.