Increased myofibrillar protein catabolism in Duchenne muscular dystrophy measured by 3-methylhistidine excretion in the urine.

نویسندگان

  • R O McKeran
  • D Halliday
  • P Purkiss
چکیده

Myofibrillar protein catabolic rate was calculated in seven patients with Duchenne muscular dystrophy from the amount of 3-methylhistidine excreted in the urine, and found to be over three times that found in a control series when expresses as the percentage of myofibrillar protein catabolised per day. It is suggested that measurement of myofibrillar protein catabolic rate may add a useful parameter in the study of muscle disorders.

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3-Methylhistidine excretion as an index of myofibrillar protein catabolism in neuromuscular disease.

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عنوان ژورنال:
  • Muscle & nerve

دوره 7 5  شماره 

صفحات  -

تاریخ انتشار 1977