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contentType Case Reports|Journal Article|Research Support, Non-U.S. Gov't
endingPage 452
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publicationName Metabolic Brain Disease
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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.
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date 2021-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language English
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title Identification of MMACHC and PROKR2 mutations causing coexistent cobalamin C disease and Kallmann syndrome in a young woman
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