Co-Authors
This is a "connection" page, showing publications co-authored by SEEMA LALANI and CHARUL GIJAVANEKAR.
Connection Strength
0.204
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Biallelic Variants in KMO Cause a Novel Form of Congenital NAD Deficiency. medRxiv. 2026 Aug 27.
Score: 0.062
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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 11; 197(11):e64177.
Score: 0.057
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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: 0.046
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Reanalysis of Clinical Exome Sequencing Data. N Engl J Med. 2019 06 20; 380(25):2478-2480.
Score: 0.038