{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T00:46:43Z","timestamp":1791334003031,"version":"4.3.1"},"reference-count":105,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2011,2,10]],"date-time":"2011-02-10T00:00:00Z","timestamp":1297296000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt C"],"published-print":{"date-parts":[[2011,2,15]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Derivatives of cobalamin (vitamin B\n                    <jats:sub>12<\/jats:sub>\n                    ) are required for activity of two enzymes in humans. Adenosylcobalamin is required for activity of mitochondrial methylmalonylCoA mutase and methylcobalamin is required for activity of cytoplasmic methionine synthase. Deficiency in cobalamin, or inability to absorb cobalamin normally, can result in accumulation of methylmalonic acid and homocysteine in blood and urine. Methylmalonic acidemia can result in metabolic acidosis which in severe cases may be fatal. Hyperhomocysteinemia along with hypomethioninemia can result in hematologic (megaloblastic anemia, neutropenia, thrombocytopenia) and neurologic (subacute combined degeneration of the cord, dementia, psychosis) defects. Inborn errors affecting cobalamin absorption (inherited intrinsic factor deficiency, Imerslund\u2013Gr\u00e4sbeck syndrome) and transport (transcobalamin deficiency) have been described. A series of inborn errors of intracellular cobalamin metabolism, designated cblA\u2010cblG, have been differentiated by complementation analysis. These can give rise to isolated methylmalonic acidemia (\n                    <jats:italic>cblA<\/jats:italic>\n                    ,\n                    <jats:italic>cblB<\/jats:italic>\n                    ,\n                    <jats:italic>cblD<\/jats:italic>\n                    variant 2), isolated hyperhomocysteinemia (\n                    <jats:italic>cblD<\/jats:italic>\n                    variant 1,\n                    <jats:italic>cblE<\/jats:italic>\n                    ,\n                    <jats:italic>cblG<\/jats:italic>\n                    ) or combined methylmalonic acidemia and hyperhomocysteinemia (\n                    <jats:italic>cblC<\/jats:italic>\n                    , classic\n                    <jats:italic>cblD<\/jats:italic>\n                    ,\n                    <jats:italic>cblF<\/jats:italic>\n                    ). All these disorders are inherited as autosomal recessive traits. The genes underlying each of these disorders have been identified. Two other disorders, haptocorrin deficiency and transcobalamin receptor deficiency, have been described, but it is not clear that they have any consistent clinical phenotype. \u00a9 2011 Wiley\u2010Liss, Inc.\n                  <\/jats:p>","DOI":"10.1002\/ajmg.c.30288","type":"journal-article","created":{"date-parts":[[2011,2,10]],"date-time":"2011-02-10T18:12:16Z","timestamp":1297361536000},"page":"33-44","source":"Crossref","is-referenced-by-count":187,"title":["Inborn errors of cobalamin absorption and metabolism"],"prefix":"10.1002","volume":"157","author":[{"given":"David","family":"Watkins","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David 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