Lauren MacNeil

3PUBLICATIONS
4CO-AUTHORS
Infant and child healthNeurogeneticsNeurology and neuromuscular diseases
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Publications (3)

|Nov 29, 2021
The Alberta Newborn Screening Approach for Sickle Cell Disease: The Advantages of Molecular Testing.

Janet R Zhou, Ross Ridsdale, Lauren MacNeil

|Sep 05, 2020
Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency.

Maian Roifman, Kirsten M Niles, Lauren MacNeil

|Nov 20, 2019
Homozygous pathogenic variant in BRAT1 associated with nonprogressive cerebellar ataxia.

Areej Mahjoub, Zuzana Cihlarova, Martine Tétreault

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