Phosphoserine aminotransferase deficiency: imaging findings in a child with congenital microcephaly
Author:
Affiliation:
1. Department of Medical Imaging, Children’s Hospital of Eastern Ontario, Ottawa, Canada;
2. Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Canada
Publisher
Informa UK Limited
Subject
Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/14767058.2018.1514375
Reference7 articles.
1. Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway
2. Congenital Microcephaly with a Simplified Gyral Pattern: Associated Findings and Their Significance
3. 3-Phosphoglycerate dehydrogenase deficiency: an inborn error of serine biosynthesis.
4. Prenatal and early postnatal treatment in 3-phosphoglycerate-dehydrogenase deficiency
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