Brivazens
Neurology India
menu-bar5 Open access journal indexed with Index Medicus
  Users online: 8407  
 Home | Login 
About Editorial board Articlesmenu-bullet NSI Publicationsmenu-bullet Search Instructions Online Submission Subscribe Videos Etcetera Contact
Read this article

 


    Article Cited by others

ORIGINAL ARTICLE

New mutation of the desmin gene identified in an extended Indian pedigree presenting with distal myopathy and cardiac disease

Nalini Atchayaram, Gayathri Narayanappa, Richard Pascale, Cobo Ana-Maria, Urtizberea J Andoni

Year : 2013| Volume: 61| Issue : 6 | Page no: 622-626

   This article has been cited by
 
1 A Novel L1 Linker Mutation in DES Resulted in Total Absence of Protein
Rashmi Santhoshkumar, Veeramani Preethish-Kumar, Kiran Polavarapu, Dinesh Reghunathan, Sima Chaudhari, Kapaettu Satyamoorthy, Seena Vengalil, Saraswati Nashi, Muhammed Faruq, Aditi Joshi, Nalini Atchayaram, Gayathri Narayanappa
Journal of Molecular Neuroscience. 2021; 71(12): 2468
[Pubmed]  [Google Scholar] [DOI]
2 Sudden cardiac death in neuromuscular disorders
Josef Finsterer,Claudia Stöllberger,Concha Maeztu
International Journal of Cardiology. 2016; 203: 508
[Pubmed]  [Google Scholar] [DOI]
3 Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect
Andreas Brodehl,Mareike Dieding,Niklas Biere,Andreas Unger,Bärbel Klauke,Volker Walhorn,Jan Gummert,Uwe Schulz,Wolfgang A. Linke,Brenda Gerull,Matthias Vorgert,Dario Anselmetti,Hendrik Milting
Journal of Molecular and Cellular Cardiology. 2016; 91: 207
[Pubmed]  [Google Scholar] [DOI]
4 Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the Nerves
Josef Finsterer,Claudia Stöllberger
Korean Circulation Journal. 2016; 46(2): 117
[Pubmed]  [Google Scholar] [DOI]

 

Online since 20th March '04
Published by Wolters Kluwer - Medknow