Sequential multiple retinal vein occlusions and transient ischemic attack in MTHFR polymorphism and protein S deficiency

BACKGROUND: The C677T variant of the MTHFR (5,10‐Methylenetetrahydrofolate reductase) gene is associated with increased susceptibility to homocystinuria (OMIM#236250), neural tube defects (OMIM#601634), schizophrenia (OMIM#181500), thromboembolism (OMIM#188050), and vascular diseases. Protein S defi...

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Detalles Bibliográficos
Autores principales: Cho, Ahra, Ragi, Sara D., Oh, Jin Kyun, Lima de Carvalho, Jose Ronaldo, Ryu, Joseph, Yang, Ber‐Yuh, Tsang, Stephen H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336745/
https://www.ncbi.nlm.nih.gov/pubmed/32347013
http://dx.doi.org/10.1002/mgg3.1273

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336745/
https://www.ncbi.nlm.nih.gov/pubmed/32347013
http://dx.doi.org/10.1002/mgg3.1273

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