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Infantile type of homocystinuria with 5,10-methylenetetrahydrofolate reductase deficiency.
Y Wada, K Narisawa, T Arakawa
Monographs in human genetics 1978
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No abstract available.
Citation
Y Wada, K Narisawa, T Arakawa.
Infantile type of homocystinuria with 5,10-methylenetetrahydrofolate reductase deficiency.
Monographs in human genetics.
1978;9:140-6
Mesh Tags
Apnea
Brain
Consanguinity
Female
Genes, Recessive
Heterozygote Detection
Homocystinuria
Homozygote
Humans
Infant
Infant, Newborn
Infant, Newborn, Diseases
Intellectual Disability
Kidney
Leukocytes
Liver
Methylenetetrahydrofolate Dehydrogenase (NADP)
Oxidoreductases
Seizures
Syndrome
Substances
Oxidoreductases
Methylenetetrahydrofolate Dehydrogenase (NADP)
PMID: 732831
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