AAAAAA

   
Results: 1-3 |
Results: 3
Mutations in COX15 Produce a Defect in the Mitochondrial Heme Biosynthetic Pathway, Causing Early-Onset Fatal Hypertrophic Cardiomyopathy
Authors: Antonicka, Hana Mattman, Andre Carlson, Christopher G. Glerum, D. Moira Hoffbuhr, Kristen C. Leary, Scot C. Kennaway, Nancy G. Shoubridge, Eric A.
Citation: Antonicka, Hana et al., Mutations in COX15 Produce a Defect in the Mitochondrial Heme Biosynthetic Pathway, Causing Early-Onset Fatal Hypertrophic Cardiomyopathy, American journal of human genetics , 72(1), 2003, pp. 101-114
Gyrate atrophy of the choroid and retina: characterization of mutant ornithine aminotransferase and mechanism of response to vitamin B6
Authors: Kennaway, Nancy G. Stankova, Libuse Wirtz, Mary K. Weleber, Richard G.
Citation: G. Kennaway, Nancy et al., Gyrate atrophy of the choroid and retina: characterization of mutant ornithine aminotransferase and mechanism of response to vitamin B6, American journal of human genetics , 44(3), 1989, pp. 344-352
Inheritance of ornithine aminotransferase gene, mrna, and enzyme defect in a family with gyrate atrophy of the choroid and retina
Authors: Hotta, Yoshihiro Kennaway, Nancy G. Weleber, Richard G. Inana, George
Citation: Hotta, Yoshihiro et al., Inheritance of ornithine aminotransferase gene, mrna, and enzyme defect in a family with gyrate atrophy of the choroid and retina, American journal of human genetics , 44(3), 1989, pp. 353-357
Risultati: 1-3 |