C9orf72 mutations may be rare in frontotemporal lobar degeneration patients in India

Amyotroph Lateral Scler Frontotemporal Degener. 2015;17(1-2):151-3. doi: 10.3109/21678421.2015.1074706. Epub 2015 Oct 14.

Authors

Odity Mukherjee¹, Gopal Das², Somdutta Sen³, Aparna Dutt⁴, Suvarna Alladi⁵, Amitabha Ghosh⁴

Affiliations

¹ a Centre for Brain Development and Repair (CBDR), Institute of Stem Cells and Regenerative Medicine , Bangalore , India .
² b Molecular Neurobiology Group (Lab 5) , National Centre for Biological Sciences , Bangalore , India .
³ c Department of Psychiatry , National Institute of Mental Health and Neurosciences , Bangalore , India .
⁴ d Department of Neurology, Cognitive Neurology Unit , Apollo Gleneagles Hospitals , Kolkata , India and.
⁵ e Department of Neurology , Nizam's Institute of Medical Sciences , Panjagutta , Hyderabad , India.

PMID: 26465714
DOI: 10.3109/21678421.2015.1074706

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Age Distribution
C9orf72 Protein
Comorbidity
Female
Frontotemporal Lobar Degeneration / epidemiology*
Frontotemporal Lobar Degeneration / genetics*
Genetic Association Studies
Genetic Markers / genetics
Genetic Predisposition to Disease / epidemiology*
Genetic Predisposition to Disease / genetics*
Humans
India / epidemiology
Male
Middle Aged
Mutation / genetics
Polymorphism, Single Nucleotide / genetics*
Prevalence
Proteins / genetics*
Reproducibility of Results
Risk Assessment / methods
Sensitivity and Specificity
Sex Distribution

Substances

C9orf72 Protein
C9orf72 protein, human
Genetic Markers
Proteins