PEX2 deficiency (Q97726): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 13:51, 16 August 2026
This refers to deficiency in the protein that is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_899078324 |
||
| English | PEX2 deficiency |
This refers to deficiency in the protein that is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease. |
Statements
CID11:ID_899078324
0 references
dki-india-ID_899078324
0 references
Concluído
0 references
15 August 2026
0 references
