The (Ala-Val) mutation of methylenetetrahydrofolate reductase as a genetic risk factor for vascular disease in non-insulin-dependent diabetic patients.

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Autoria(s): Brulhart M.C.; Dussoix P.; Ruiz J.; Passa P.; Froguel P.; James R.W.

Data(s)	1997
Identificador	http://serval.unil.ch/?id=serval:BIB_FAA8E68186C2 isbn:0002-9297 pmid:8981966 isiid:A1997WA81800029
Idioma(s)	en
Fonte	American journal of human genetics, vol. 60, no. 1, pp. 228-9
Palavras-Chave	#Coronary Disease; Diabetes Mellitus, Type 2; Diabetic Angiopathies; Gene Frequency; Genotype; Humans; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Risk Factors
Tipo	info:eu-repo/semantics/article article