Coenzyme Q10 Deficiency and Type 2C Muscle Fibers

Coenzyme Q10 Deficiency and Type 2C Muscle Fibers

Investigators at Washington University School of Medicine, St Louis, MO, evaluated retrospectively clinical, laboratory, and muscle histochemistry and oxidative enzyme characteristics in 49 children with suspected mitochondrial disorders.

Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2013-12-01
Series:Pediatric Neurology Briefs
Subjects:
type 2c muscle fibers
coq10 deficiency
morphologically normal muscle
Online Access:https://www.pediatricneurologybriefs.com/articles/355
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spelling doaj-16b5479c98834a9185f10b493d7ec8bf2020-11-25T02:41:50ZengPediatric Neurology Briefs PublishersPediatric Neurology Briefs1043-31552166-64822013-12-012712969610.15844/pedneurbriefs-27-12-9341Coenzyme Q10 Deficiency and Type 2C Muscle FibersJ Gordon Millichap0Northwestern University Feinberg School of MedicineInvestigators at Washington University School of Medicine, St Louis, MO, evaluated retrospectively clinical, laboratory, and muscle histochemistry and oxidative enzyme characteristics in 49 children with suspected mitochondrial disorders.https://www.pediatricneurologybriefs.com/articles/355type 2c muscle fiberscoq10 deficiencymorphologically normal muscle
collection DOAJ
language English
format Article
sources DOAJ
author J Gordon Millichap
spellingShingle J Gordon Millichap
Coenzyme Q10 Deficiency and Type 2C Muscle Fibers
Pediatric Neurology Briefs
type 2c muscle fibers
coq10 deficiency
morphologically normal muscle
author_facet J Gordon Millichap
author_sort J Gordon Millichap
title Coenzyme Q10 Deficiency and Type 2C Muscle Fibers
title_short Coenzyme Q10 Deficiency and Type 2C Muscle Fibers
title_full Coenzyme Q10 Deficiency and Type 2C Muscle Fibers
title_fullStr Coenzyme Q10 Deficiency and Type 2C Muscle Fibers
title_full_unstemmed Coenzyme Q10 Deficiency and Type 2C Muscle Fibers
title_sort coenzyme q10 deficiency and type 2c muscle fibers
publisher Pediatric Neurology Briefs Publishers
series Pediatric Neurology Briefs
issn 1043-3155
2166-6482
publishDate 2013-12-01
description Investigators at Washington University School of Medicine, St Louis, MO, evaluated retrospectively clinical, laboratory, and muscle histochemistry and oxidative enzyme characteristics in 49 children with suspected mitochondrial disorders.
topic type 2c muscle fibers
coq10 deficiency
morphologically normal muscle
url https://www.pediatricneurologybriefs.com/articles/355
work_keys_str_mv AT jgordonmillichap coenzymeq10deficiencyandtype2cmusclefibers
_version_ 1724777098608902144

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