MTHFRpolymorphismmutationTaqman probeGuanglu CheDepartment of Laboratory Medicine, West China Second University Hospital, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, P.R. ...
The prevalence of MTHFR A1298C genotype is population-specific, implying that permissive geneenvironment interactions other than genetic mutation alone may also be relevant in establishing a clinically overt disease. Causality remains to be proven in prospective evaluation across diverse geographic areas ...
Acquired Thrombotic Thrombocytopenic Purpura (TTP) in a patient with heterozygous MTHFR C677T mutation and hyperhomocysteinemia – a case reportAcquired Thrombotic Thrombocytopenic PurpuraMTHFR C677T mutationdoi:10.1016/j.achaem.2015.07.112elsevier
8 Martinez Saguer I, Escuriola Ettingshausen C. Successful management of hereditary angioedema during pregnancy in a patient with heterozygous MTHFR mutation.doi:10.1111/dth.14541Maddalena NapolitanoMaria VastarellaGabriella FabbrociniEleonora Cinelli...
Successful management of hereditary angioedema during pregnancy in a patient with heterozygous MTHFR mutationdoi:10.1016/j.anai.2017.04.001Inmaculada Martinez SaguerCarmen Escuriola EttingshausenAnnals of Allergy, Asthma & Immunology