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Maya Mary Thomas

Showing results (21-30 of 24) with videos related to

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American Journal of Medical Genetics. Part A|May 3, 2025
A Novel Presentation and Variable Phenotypic Spectrum of Homozygous Start-Loss Variant in LYRM7-Associated Mitochondrial Complex III DeficiencyNoel Deep Luke, Aditya Vijayakrishnan Nair, Ajith Sivadasan, et al.
Neurochemistry International|December 30, 2019
Phosphoproteomic analysis reveals Akt isoform-specific regulation of cytoskeleton proteins in human temporal lobe epilepsy with hippocampal sclerosisRajesh Ramanna Valmiki, Subhashini Venkatesalu, Ari George Chacko, et al.
The Lancet Regional Health. Southeast Asia|June 11, 2025
Neuromelioidosis outbreak in Tamil Nadu, India: an investigation of transmission with genomic insightsAngel Miraclin Thirugnanakumar, Prabu Rajkumar, Karthik Gunasekaran, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
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Showing results (21-30 of 24) with videos related to

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Pageof 3
You have reached the last page of results.This site can display upto 24 results.
American Journal of Medical Genetics. Part A|May 3, 2025
A Novel Presentation and Variable Phenotypic Spectrum of Homozygous Start-Loss Variant in LYRM7-Associated Mitochondrial Complex III DeficiencyNoel Deep Luke, Aditya Vijayakrishnan Nair, Ajith Sivadasan, et al.
Neurochemistry International|December 30, 2019
Phosphoproteomic analysis reveals Akt isoform-specific regulation of cytoskeleton proteins in human temporal lobe epilepsy with hippocampal sclerosisRajesh Ramanna Valmiki, Subhashini Venkatesalu, Ari George Chacko, et al.
The Lancet Regional Health. Southeast Asia|June 11, 2025
Neuromelioidosis outbreak in Tamil Nadu, India: an investigation of transmission with genomic insightsAngel Miraclin Thirugnanakumar, Prabu Rajkumar, Karthik Gunasekaran, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
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