bibliographicCitation |
Yuan H, Deng S, Gao W, Li H, Yuan M. Identification of MMACHC and PROKR2 mutations causing coexistent cobalamin C disease and Kallmann syndrome in a young woman. Metab Brain Dis. 2021 Mar;36(3):447–52. doi: 10.1007/s11011-020-00654-8. PMID: 33411215. |