Defective [U-14 C] palmitic acid oxidation in duchenne muscular dystrophy

James E. Carroll; Beverly J. Norris; Michael H. Brooke

doi:10.1212/wnl.35.1.96

Defective [U-14 C] palmitic acid oxidation in duchenne muscular dystrophy

James E. Carroll, Beverly J. Norris, Michael H. Brooke

Child Neurology

Research output: Contribution to journal › Article › peer-review

21 Scopus citations

Abstract

Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased [U-14 C] palmitic acid oxidation. [l-14 C] palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.

Original language	English (US)
Pages (from-to)	96-97
Number of pages	2
Journal	Neurology
Volume	35
Issue number	1
DOIs	https://doi.org/10.1212/wnl.35.1.96
State	Published - Jan 1985

ASJC Scopus subject areas

Clinical Neurology

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title = "Defective [U-14 C] palmitic acid oxidation in duchenne muscular dystrophy",

abstract = "Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased [U-14 C] palmitic acid oxidation. [l-14 C] palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.",

author = "Carroll, {James E.} and Norris, {Beverly J.} and Brooke, {Michael H.}",

year = "1985",

month = jan,

doi = "10.1212/wnl.35.1.96",

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AU - Carroll, James E.

AU - Norris, Beverly J.

AU - Brooke, Michael H.

PY - 1985/1

Y1 - 1985/1

N2 - Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased [U-14 C] palmitic acid oxidation. [l-14 C] palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.

AB - Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased [U-14 C] palmitic acid oxidation. [l-14 C] palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.

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EP - 97

JO - Neurology

JF - Neurology

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Defective [U-14 C] palmitic acid oxidation in duchenne muscular dystrophy

Abstract

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