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Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.
Leclerc, D; Campeau, E; Goyette, P; Adjalla, C E; Christensen, B; Ross, M; Eydoux, P; Rosenblatt, D S; Rozen, R; Gravel, R A.
Affiliation
  • Leclerc D; MRC Group in Medical Genetics, Department of Pediatrics, McGill University, Montreal, Quebec, Canada.
Hum Mol Genet ; 5(12): 1867-74, 1996 Dec.
Article in En | MEDLINE | ID: mdl-8968737
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Collection: 01-internacional Database: MEDLINE Main subject: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase / Vitamin B 12 / Chromosomes, Human, Pair 1 / DNA, Complementary / Amino Acid Metabolism, Inborn Errors / Homocysteine Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 1996 Document type: Article Affiliation country: Country of publication:
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase / Vitamin B 12 / Chromosomes, Human, Pair 1 / DNA, Complementary / Amino Acid Metabolism, Inborn Errors / Homocysteine Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 1996 Document type: Article Affiliation country: Country of publication: