Načítá se...
Identification of a Novel GLA Mutation (L206 P) in a Patient with Fabry Disease
We report a new α-Galactosidase A (αGal-A) mutation in a 39-year-old Korean born, male Fabry disease patient. Fabry disease is a devastating, progressive inborn error of metabolism caused by X-linked genetic mutations. In this case, the first clinical symptom to occur was in childhood consisting of...
Uloženo v:
| Vydáno v: | Korean Circ J |
|---|---|
| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Korean Society of Cardiology
2017
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5378036/ https://ncbi.nlm.nih.gov/pubmed/28382085 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4070/kcj.2016.0321 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|