Compound heterozygosity for the C677T and A1298C mutations of the MTHFR gene in a case of hyperhomocysteinemia with recurrent deep thrombosis at young age.

Romanian journal of internal medicine = Revue roumaine de médecine interne

Volumn 46, Issue 3, 2008, Pages 255-259

  Jurcuţ, Ruxandra ^a   Pop, Ioana ^a   Coriu, D ^a   Grasu, M ^a   Zilişteanu, Diana ^a   Giusca S ^a   Ginghinǎ, Carmen ^a  

^a Prof Dr C C Iliescu Emergency Institute of Cardiovascular Diseases   (Romania)

Author keywords

[No Author keywords available]

Indexed keywords

METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);

ADULT; ARTICLE; CASE REPORT; FEMALE; GENETICS; HETEROZYGOTE; HUMAN; HYPERHOMOCYSTEINEMIA; SINGLE NUCLEOTIDE POLYMORPHISM; VEIN THROMBOSIS;

FEMALE; HETEROZYGOTE; HUMANS; HYPERHOMOCYSTEINEMIA; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); POLYMORPHISM, SINGLE NUCLEOTIDE; VENOUS THROMBOSIS; YOUNG ADULT;

EID: 65549169940     PISSN: 12204749     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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