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1-3 of 3 results for NEMMLAS

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Select article: Expanding the Phenotype: Neurodevelopmental Disorder,Mitochondrial,With Abnormal Movements and Lactic Acidosis,With or Without Seizures (NEMMLAS) due to WARS2 Biallelic Variants,Encoding Mitochondrial Tryptophanyl-tRNA Synthase

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First published 2019-10

Expanding the Phenotype: Neurodevelopmental Disorder,Mitochondrial,With Abnormal Movements and Lactic Acidosis,With or Without Seizures (NEMMLAS) due to WARS2 Biallelic Variants,Encoding Mitochondrial Tryptophanyl-tRNA Synthase

Manveen Virdee, Eroshini Swarnalingam, Mariya Kozenko [...]

Journal of Child Neurology

Select article: NEMMLAS Due to Biallelic WARS2 Variants

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Other

First published 2020-2

NEMMLAS Due to Biallelic WARS2 Variants

Josef Finsterer

Journal of Child Neurology

Select article: Expanding the Phenotype: Neurodevelopmental Disorder,Mitochondrial,With Abnormal Movements and Lactic Acidosis,With or Without Seizures (NEMMLAS) Due to WARS2 Biallelic Variants,Encoding Mitochondrial Tryptophanyl-tRNA Synthase

Retricted access

Other

First published 2020-2

Expanding the Phenotype: Neurodevelopmental Disorder,Mitochondrial,With Abnormal Movements and Lactic Acidosis,With or Without Seizures (NEMMLAS) Due to WARS2 Biallelic Variants,Encoding Mitochondrial Tryptophanyl-tRNA Synthase

Mark Tarnopolsky, Mariya Kozenko, Kevin Jones

Journal of Child Neurology

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