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Diabetes Care|November 14, 1997
Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Comparison with MIDD syndrome (A3243G mutation): a case reportB H Vialettes, V Paquis-Flucklinger, J F Pelissier, et al.
Diagnostic and Interventional Imaging|July 24, 2019
Assessment of proximal femur microarchitecture using ultra-high field MRI at 7 TeslaD Guenoun, M Pithioux, J-C Souplet, et al.
Neuromuscular Disorders : NMD|February 5, 2013
In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotypeC Gineste, J M De Winter, C Kohl, et al.
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