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Results: 1-5 |
Results: 5

Authors: OSAKI Y NISHINO I MURAKAMI N MATSUBAYASHI K TSUDA K YOKOYAMA YI MORITA M ONISHI S GOTO YI NONAKA I
Citation: Y. Osaki et al., MITOCHONDRIAL ABNORMALITIES IN SELENIUM-DEFICIENT MYOPATHY, Muscle & nerve, 21(5), 1998, pp. 637-639

Authors: NISHINO I KOBAYASHI O GOTO YI KURIHARA M KUMAGAI K FUJITA T HASHIMOTO K HORAI S NONAKA I
Citation: I. Nishino et al., A NEW CONGENITAL MUSCULAR-DYSTROPHY WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES, Muscle & nerve, 21(1), 1998, pp. 40-47

Authors: HUIE ML TSUJINO S BROOKS SS ENGEL A ELIAS E BONTHRON DT BESSLEY C SHANSKE S DIMAURO S GOTO YI HIRSCHHORN R
Citation: Ml. Huie et al., GLYCOGEN-STORAGE-DISEASE TYPE-II - IDENTIFICATION OF 4 NOVEL MISSENSEMUTATIONS (D645N, G648S, R672W, R672Q) AND 2 INSERTIONS DELETIONS IN THE ACID ALPHA-GLUCOSIDASE LOCUS OF PATIENTS OF DIFFERING PHENOTYPE/, Biochemical and biophysical research communications, 244(3), 1998, pp. 921-927

Authors: GOTO YI NISHINO I HORAI S NONAKA I
Citation: Yi. Goto et al., DETECTION OF DNA FRAGMENTS ENCOMPASSING THE DELETION JUNCTION OF MITOCHONDRIAL GENOME, Biochemical and biophysical research communications, 222(2), 1996, pp. 215-219

Authors: GOTO YI TSUGANE K TANABE Y NONAKA I HORAI S
Citation: Yi. Goto et al., A NEW POINT MUTATION AT NUCLEOTIDE PAIR-3291 OF THE MITOCHONDRIAL TRANSFER-RNA(LEU(UUR)) GENE IN A PATIENT WITH MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES (MELAS), Biochemical and biophysical research communications, 202(3), 1994, pp. 1624-1630
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