Phosphorus‐31 magnetic resonance spectroscopy of skeletal muscle in maternally inherited diabetes and deafness A3243G mitochondrial mutation carriers
Phosphorus‐31 magnetic resonance spectroscopy of skeletal muscle in maternally inherited diabetes and deafness A3243G mitochondrial mutation carriers
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DOI：
10.1002/jmri.21620
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发表时间：
2009-01
影响因子：
4.4
通讯作者：
S. V. van Elderen;J. Doornbos;E. Van Essen;H. Lemkes;J. Maassen;Jan W. A. Smit;A. de Roos
中科院分区：
文献类型：
--
作者：
S. V. van Elderen;J. Doornbos;E. Van Essen;H. Lemkes;J. Maassen;Jan W. A. Smit;A. de Roos
研究母系遗传性糖尿病和耳聋（MIDD）综合征患者横纹肌中的高能磷酸盐代谢。
To investigate high‐energy phosphate metabolism in striated skeletal muscle of patients with Maternally Inherited Diabetes and Deafness (MIDD) syndrome.