Home About us Articles Multimedia Search Instructions Login 
IF 2017: 1.596 (® Clarivate Analytics)
Total Cites: 7606
Q2 in Medicine, General & Internal
Follow Us
Follow Us
  • Users Online: 1020
  • Home
  • Print this page
  • Email this page

    Article Cited by others


A Novel Missense Mutation in the Spectrin Beta Nonerythrocytic 2 Gene Likely Associated with Spinocerebellar Ataxia Type 5

Liu Li-Zhi, Ren Ming, Li Mao, Ren Yu-Ting, Sun Bo, Sun Xiao-Sun, Chen Si-Yu, Li Si-Yuan, Huang Xu-Sheng

Year : 2016| Volume: 129| Issue : 20 | Page no: 2516-2517

   This article has been cited by
1 Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypes
Miao Sun,Amy Knight Johnson,Viswateja Nelakuditi,Lucia Guidugli,David Fischer,Kelly Arndt,Lan Ma,Erin Sandford,Vikram Shakkottai,Kym Boycott,Jodi Warman Chardon,Zejuan Li,Daniela del Gaudio,Margit Burmeister,Christopher M. Gomez,Darrel J. Waggoner,Soma Das
Genetics in Medicine. 2018;
[Pubmed]  [Google Scholar] [DOI]
2 A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature
Mohammad A. Al-Muhaizea,Faten AlMutairi,Rawan Almass,Safinaz AlHarthi,Mazhor S. Aldosary,Maysoon Alsagob,Ali AlOdaib,Dilek Colak,Namik Kaya
The Cerebellum. 2017;
[Pubmed]  [Google Scholar] [DOI]
3 -III-spectrin spinocerebellar ataxia type 5 mutation reveals a dominant cytoskeletal mechanism that underlies dendritic arborization
Adam W. Avery,David D. Thomas,Thomas S. Hays
Proceedings of the National Academy of Sciences. 2017; : 201707108
[Pubmed]  [Google Scholar] [DOI]


Read this article