Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD) - Concepedia

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Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD)

DOI Full Paper Access

23

Citations

33

References

2016

Year

Shanti Balasubramaniam, Brandon Lewis, D M Mock, Hamid M. Said, Maja Tarailo‐Graovac, André Mattman, Clara D.M. van Karnebeek, David R. Thorburn, Richard J. Rodenburg, John Christodoulou

References

	Year	Citations

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