Low citrulline in Leigh disease: still a biomarker of maternally inherited Leigh syndrome.
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A guide to diagnosis and treatment of Leigh syndrome.Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD).m.8993T>G-Associated Leigh Syndrome with Hypocitrullinemia on Newborn Screening.Mitochondrial DNA 8993T>G mutation in a child with ornithine transcarbamylase deficiency and leigh syndrome: an unexpected association.Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA Mutations
P2860
Low citrulline in Leigh disease: still a biomarker of maternally inherited Leigh syndrome.
description
2010 nî lūn-bûn
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name
Low citrulline in Leigh diseas ...... ally inherited Leigh syndrome.
@en
Low citrulline in Leigh diseas ...... ally inherited Leigh syndrome.
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type
label
Low citrulline in Leigh diseas ...... ally inherited Leigh syndrome.
@en
Low citrulline in Leigh diseas ...... ally inherited Leigh syndrome.
@nl
prefLabel
Low citrulline in Leigh diseas ...... ally inherited Leigh syndrome.
@en
Low citrulline in Leigh diseas ...... ally inherited Leigh syndrome.
@nl
P2093
P2860
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P1476
Low citrulline in Leigh diseas ...... ally inherited Leigh syndrome.
@en
P2093
François-Guillaume Debray
Grant A Mitchell
Marie Lambert
Pierre Allard
P2860
P304
P356
10.1177/0883073809351983
P577
2010-05-14T00:00:00Z