Co-Authors
This is a "connection" page, showing publications co-authored by SEEMA LALANI and CHARUL GIJAVANEKAR.
Connection Strength
0.151
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A Rare Molecular Diagnosis in a Patient With Hepatocerebral Syndrome Contributes to the Expansion of the Phenotypic Spectrum of POLG2-Related Mitochondrial Disorder. Am J Med Genet A. 2025 Jul 09; e64177.
Score: 0.061
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Niacin therapy improves outcome and normalizes metabolic abnormalities in an NAXD-deficient patient. Brain. 2022 06 03; 145(5):e36-e40.
Score: 0.050
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Reanalysis of Clinical Exome Sequencing Data. N Engl J Med. 2019 06 20; 380(25):2478-2480.
Score: 0.040