Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases
There are two genetically determined biotin-dependent disorders. The first is holocarboxylase synthetase (HCS) deficiency and the second biotinidase deficiency. HCS catalyzes the reaction in which active holocarboxylases are synthesized from inactive apocarboxylases. Biotin is required for th...
| Egile Nagusiak: | , , |
|---|---|
| Formatua: | Artikulua |
| Hizkuntza: | English |
| Argitaratua: |
Hacettepe University Institute of Child Health
1994-10-01
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| Saila: | The Turkish Journal of Pediatrics |
| Sarrera elektronikoa: | https://turkjpediatr.org/article/view/3638 |