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Published in: Child's Nervous System 4/2018

01-04-2018 | Letter to the Editor

Cerebellar atrophy with T2/FLAIR hyperintense cerebellar cortex: a new imaging phenotype of combined complex II/III deficiency

Authors: Ai Peng Tan, Carlos Robles, Kshitij Mankad

Published in: Child's Nervous System | Issue 4/2018

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Excerpt

Dear Editor: …
Literature
4.
go back to reference Parfait B, Chretien D, Rötig A, Marsac C, Munnich A et al (2000) Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome. Hum Genet 106:236–243CrossRefPubMed Parfait B, Chretien D, Rötig A, Marsac C, Munnich A et al (2000) Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome. Hum Genet 106:236–243CrossRefPubMed
Metadata
Title
Cerebellar atrophy with T2/FLAIR hyperintense cerebellar cortex: a new imaging phenotype of combined complex II/III deficiency
Authors
Ai Peng Tan
Carlos Robles
Kshitij Mankad
Publication date
01-04-2018
Publisher
Springer Berlin Heidelberg
Published in
Child's Nervous System / Issue 4/2018
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-018-3762-5

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