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Literature summary for 1.8.3.7 extracted from
- Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme (2003), Cell, 113, 435-444.
Cloned(Commentary)
| Cloned (Comment) | Organism |
|---|---|
- |
Homo sapiens |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | Q8NBK3 | - |
- |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| C-alpha-formylglycine-generating enzyme 1 | - |
Homo sapiens |
| SUMF1 | - |
Homo sapiens |
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Release 2023.1 (January 2023)
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