Co-Authors
This is a "connection" page, showing publications co-authored by SEEMA LALANI and PENELOPE BONNEN.
Connection Strength
0.424
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Personalized medicine approach confirms a milder case of ABAT deficiency. Mol Brain. 2016 12 01; 9(1):93.
Score: 0.144
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Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations. Am J Hum Genet. 2016 Feb 04; 98(2):347-57.
Score: 0.135
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TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. Am J Hum Genet. 2013 Aug 08; 93(2):197-210.
Score: 0.113
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The GABA transaminase, ABAT, is essential for mitochondrial nucleoside metabolism. Cell Metab. 2015 Mar 03; 21(3):417-27.
Score: 0.032