Functional and morphological abnormalities of mitochondria harbouring the tRNALeu(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease

✍ Scribed by J. M. W. van den Ouweland; P. Maechler; C. B. Wollheim; G. Attardi; J. A. Maassen

• Publisher: Springer
• Year: 1999
• Tongue: English
• Weight: 230 KB
• Volume: 42
• Category: Article
• ISSN: 0012-186X
• DOI: 10.1007/s001250051183