Nicholls D P, Campbell N P, Stevenson H P, Patterson V H
Royal Victoria Hospital, Belfast Northern Ireland.
Heart. 1996 Oct;76(4):372-3. doi: 10.1136/hrt.76.4.372.
McArdle's disease (myophosphorylase deficiency) results in the inability to metabolise skeletal muscle glycogen to lactate. A patient with this condition developed angina and therefore offered a unique opportunity to explore the differential expression of the defective myophosphorylase gene in skeletal and cardiac muscle.
麦克尔憩室病(肌磷酸化酶缺乏症)导致无法将骨骼肌糖原代谢为乳酸。一名患有这种疾病的患者出现了心绞痛,因此提供了一个独特的机会来探索有缺陷的肌磷酸化酶基因在骨骼肌和心肌中的差异表达。