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Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India.
Adv Biol (Weinh). 2022 Nov;6(11):e2101326. doi: 10.1002/adbi.202101326. Epub 2022 Jul 10.
Adv Biol (Weinh). 2022.
PMID: 35810474
Successful renal transplantation in a family with a novel mutation in COL4A3 gene and autosomal recessive Alport syndrome.
Girimaji N, Murugan Sm S, Nada R, Sharma A, Rathi M, Kohli HS, Gupta KL, Ramachandran R.
Girimaji N, et al. Among authors: murugan sm s.
Nephrology (Carlton). 2020 Jun;25(6):497-501. doi: 10.1111/nep.13693. Epub 2020 Jan 29.
Nephrology (Carlton). 2020.
PMID: 31925849
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A cancer vaccine approach for personalized treatment of Lynch Syndrome.
Majumder S, Shah R, Elias J, Manoharan M, Shah P, Kumari A, Chakraborty P, Kode V, Mistry Y, Coral K, Mittal B, Sm SM, Mahadevan L, Gupta R, Chaudhuri A, Khanna-Gupta A.
Majumder S, et al. Among authors: sm sm.
Sci Rep. 2018 Aug 14;8(1):12122. doi: 10.1038/s41598-018-30466-x.
Sci Rep. 2018.
PMID: 30108227
Free PMC article.
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Carrier detection in Duchenne muscular dystrophy using molecular methods.
Sakthivel Murugan SM, Arthi C, Thilothammal N, Lakshmi BR.
Sakthivel Murugan SM, et al.
Indian J Med Res. 2013 Jun;137(6):1102-10.
Indian J Med Res. 2013.
PMID: 23852291
Free PMC article.
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