Co-Authors
This is a "connection" page, showing publications co-authored by CHAYA MURALI and BRENDAN LEE.
Connection Strength
0.166
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Diagnosis of ALG12-CDG by exome sequencing in a case of severe skeletal dysplasia. Mol Genet Metab Rep. 2014; 1:213-219.
Score: 0.104
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Multi-generational mitochondrial complex V deficiency due to the recurrent ATP5F1A c.620G>A?(p.Arg207His) pathogenic variant: A novel family and a review of the literature. Mol Genet Metab. 2026 Jul 14; 149(1-2):110207.
Score: 0.062