Sequential multiple retinal vein occlusions and transient ischemic attack in MTHFR polymorphism and protein S deficiency
Abstract 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. Protei...
Main Authors: | Ahra Cho, Sara D. Ragi, Jin Kyun Oh, Jose Ronaldo Lima de Carvalho Jr, Joseph Ryu, Ber‐Yuh Yang, Stephen H. Tsang |
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Format: | Article |
Language: | English |
Published: |
Wiley
2020-07-01
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Series: | Molecular Genetics & Genomic Medicine |
Subjects: | |
Online Access: | https://doi.org/10.1002/mgg3.1273 |
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