Dhaarini Mohan
Bengaluru, KA, India
Last Updated: 09/26/2026
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Found 8 publications
Distinct and Recognisable Muscle MRI Pattern in a Series of Adults Harbouring an Identical GMPPB Gene Mutation.
Journal: Journal of neuromuscular diseases
Published: October 11, 2021
Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India.
Journal: Global medical genetics
Published: July 07, 2021
Mutation Spectrum of Primary Lipid Storage Myopathies.
Journal: Annals of Indian Academy of Neurology
Published: April 18, 2021
Comparison of The Carrier Frequency of Pathogenic Variants of DMD Gene in an Indian Cohort.
Journal: Journal of neuromuscular diseases
Published: April 12, 2021
Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome.
Journal: Journal of human genetics
Published: January 05, 2021
Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review.
Journal: Journal of clinical neurology (Seoul, Korea)
Published: September 28, 2020
Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes - A recognizable clinical phenotype.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: August 26, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026