14O Inherited neuromuscular disorders in India: Outcomes of 1000 probands in the ICGNMD study at AIIMS New Delhi
Y.V. Venugopalan(All India Institute of Medical Sciences), P. Srivastava(All India Institute of Medical Sciences), V. Straub(Newcastle upon Tyne Hospitals NHS Foundation Trust), Margaret C. Reilly, H. Houlden(National Hospital for Neurology and Neurosurgery), W. Macken(National Hospital for Neurology and Neurosurgery), A. Reyaz(All India Institute of Medical Sciences), Karthik Bharadwaj Tallapaka(Centre for Cellular and Molecular Biology), Jana Vandrovcová(Texas Tech University), Nisha Rani(University of Delhi), Renu Bhatia(All India Institute of Medical Sciences), Richard J.L.F. Lemmers(Leiden University Medical Center), Kumarasamy Thangaraj(Centre for Cellular and Molecular Biology), Lindsay A. Wilson(University of North Carolina at Chapel Hill), Tauseef Ahmad(All India Institute of Medical Sciences), N. Dominik(National Hospital for Neurology and Neurosurgery), Robert D. S. Pitceathly(National Hospital for Neurology and Neurosurgery), Ajit K. Dalal, Michael G. Hanna(National Hospital for Neurology and Neurosurgery)
Cited by 0
Related Papers
Ensembl 2012
|Nucleic Acids Research|2011|839
Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences
|Briefings in Bioinformatics|2016|815
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
|Nature Genetics|2011|635
Ensembl 2011
|Nucleic Acids Research|2010|600
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia
|Nature Genetics|2019|592