Human Methionine Synthase: cDNA Cloning and Identification of Mutations in Patients of the cblG Complementation Group of Folate/Cobalamin Disorders.
| Autor: | Leclerc, D., Campeau, E., Goyette, P., Adjalla, C. E., Christensen, B., Ross, M., Eydoux, P., Rosenblatt, D. S., Rozen, R., Gravel, R. A. |
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| Zdroj: | Human Molecular Genetics; Dec1996, Vol. 5 Issue 12, p1867-1874, 8p |
| Databáze: | Complementary Index |
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