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cps1
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- The CPS1 gene provides instructions for making the enzyme carbamoyl phosphate synthetase I. This enzyme participates in the urea cycle, a series of reactions ...
- ... About This Health Condition CA21H CAH1 CP21A_HUMAN CPS1 CYP21 CYP21B Cytochrome P450 Family 21 Subfamily A ...
- ... of Urea Cycle Disorders Types of UCD's OTC & CPS1 ASL/ASA Citrullinemia Arginase NAGS Citrin Deficiency Recognize ... transplant v. medical management Disorder Specific Research OTC & CPS1 ASL/ASA Citrullinemia NAGS Scientific Conferences and Symposia ...
- ... 000 newborns in that country. Mutations in the CPS1 gene cause carbamoyl phosphate synthetase I deficiency. The CPS1 gene provides instructions for making the enzyme carbamoyl ...
- Overview of Barth Syndrome (Barth Syndrome Foundation)Mitochondrial Diseases/Specifics ... Mitochondrial Diseases ... Barth Syndrome Foundation
- Infant with Rare, Incurable Disease Is First to Successfully Receive Personalized Gene Therapy Treatment
(National Institutes of Health)
Genes and Gene Therapy/Statistics and Research ... Genes and Gene Therapy ... National Institutes of Health ... From the National Institutes of Health ... NIH-supported gene- ...