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Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood.
N Engl J Med. 1988 Jun 30; 318(26):1738-41.NEJM

Authors+Show Affiliations

Carmel R
Department of Medicine, University of Southern California School of Medicine, Los Angeles, CA 90033.
Watkins D
No affiliation info available
Goodman SI
No affiliation info available
Rosenblatt DS
No affiliation info available

MeSH

5-Methyltetrahydrofolate-Homocysteine S-MethyltransferaseAdultDiagnosis, DifferentialFemaleHomocystinuriaHumansMethylmalonic AcidMethylmalonyl-CoA MutaseMultiple SclerosisMutationNervous System DiseasesVitamin B 12Vitamin B 12 Deficiency

Pub Type(s)

Case Reports
Journal Article
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

2897628

Citation

Carmel, R, et al. "Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood." The New England Journal of Medicine, vol. 318, no. 26, 1988, pp. 1738-41.
Carmel R, Watkins D, Goodman SI, et al. Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood. N Engl J Med. 1988;318(26):1738-41.
Carmel, R., Watkins, D., Goodman, S. I., & Rosenblatt, D. S. (1988). Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood. The New England Journal of Medicine, 318(26), 1738-41.
Carmel R, et al. Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood. N Engl J Med. 1988 Jun 30;318(26):1738-41. PubMed PMID: 2897628.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood. AU - Carmel,R, AU - Watkins,D, AU - Goodman,S I, AU - Rosenblatt,D S, PY - 1988/6/30/pubmed PY - 1988/6/30/medline PY - 1988/6/30/entrez SP - 1738 EP - 41 JF - The New England journal of medicine JO - N Engl J Med VL - 318 IS - 26 SN - 0028-4793 UR - https://www.unboundmedicine.com/medline/citation/2897628/Hereditary_defect_of_cobalamin_metabolism__cblG_mutation__presenting_as_a_neurologic_disorder_in_adulthood_ DB - PRIME DP - Unbound Medicine ER -