Case Reports
doi: 10.1056/NEJM198806303182607.
Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood
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- PMID: 2897628
- DOI: 10.1056/NEJM198806303182607
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Case Reports
Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood
N Engl J Med.
.
No abstract available
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