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	India Karnataka Ashte Bangalore

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RNASEH2C gene | Semantic Scholar

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Malavika Hebbar, Anil Kanthi, +6 authors Anju Shukla; American journal of medical genetics. Part A; Aicardi-Goutières syndrome is an early-onset severe neurological disorder characterized by intracranial calcification, white… (More). Is this relevant? Antisense transcription regulates the expression of ...

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LinkedIn: Anil Kanthi - Scientist - Clinical Diagnostics - Strand Life Sciences ...

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MySpace Profile: Anil Kanthi (anilkanthi)

Ashte, Karnataka, India

Private Homepages

ANIL KANTHI - YouTube

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Teile deine Videos mit Freunden, Verwandten oder der ganzen Welt

User ANIL KANTHI - Stack Overflow

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ANIL KANTHI Apparently, this user prefers to keep an air of mystery about them. 0 answers 1 question ~

Scientific Publications

Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a...

www.ncbi.nlm.nih.gov

Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome. Anju Shukla,1 Malavika Hebbar,1 Anshika Srivastava,2 Rajagopal Kadavigere,3 Priyanka Upadhyai,1Anil Kanthi,1 Oliver Brandau,4 Stephanie Bielas,2 and Katta M Girisha1,* ...

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Anil Kanthi | LinkedIn

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View Anil Kanthi’s professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Anil Kanthi discover inside ...

ANIL KANTHI | Manipal Academy of Higher Education - Academia.edu

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openSNP | Anil Kanthi's page

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Anil Kanthi's page. Anil has uploaded genotyping rawdata. Download this set (23andme-exome-vcf) Description. This user has not entered a description yet. Anil's ...

Aicardi-Goutieres syndrome: A genetic disorder which mimics...

www.neurologyindia.com

Neurol India is an peer-reviewed biomedical periodical of Neurological Society of India.

23andMe Index page

www.ianlogan.co.uk

The openSNP website has the details of 23andMe data sets that have been submitted to the site ... V3 mtDNA - R5a Anil Kanthi - not V

openSNP | Achievements

opensnp.org

Anil Kanthi: :51: 5809: Christoph Steinbeck: :30: 5812: trurl66: :38: 5821: Staci : :53: 5825: Deborah Frierson ...

p.Arg69Trp in RNASEH2C is a founder variant in three Indian families...

manipal.pure.elsevier.com

p.Arg69Trp in RNASEH2C is a founder variant in three Indian families with Aicardi–Goutières syndrome. Malavika Hebbar, Anil Kanthi, Aroor Shrikiran, Snehal Patil, Mamta Muranjan, Febi Francis, Vishnu Bhat B, Katta M. Girisha, Anju Shukla · Department of Medical Genetics, Kasturba Medical College, ...

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