Sepsis-like cerebrovascular event in a newborn with MTHFR homozygous mutation. [electronic resource]
Producer: 20101213Description: 499-500 p. digitalISSN:- 1442-200X
- Cerebrovascular Disorders -- diagnosis
- Electroencephalography
- Follow-Up Studies
- Gene Expression Regulation, Developmental
- Genetic Predisposition to Disease
- Heterozygote
- Homozygote
- Humans
- Infant, Newborn
- Male
- Methylenetetrahydrofolate Reductase (NADPH2) -- genetics
- Mutation
- Pedigree
- Seizures -- diagnosis
- Sepsis -- complications
No physical items for this record
Publication Type: Case Reports; Letter
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