Lataa...
A mutation in the UBIAD1 gene in a Han Chinese family with Schnyder corneal dystrophy
PURPOSE: To identify the molecular defect in the UbiA prenyltransferase domain containing 1 (UBIAD1) gene in a four-generation Chinese family with Schnyder corneal dystrophy (SCD). METHODS: A four-generation Chinese family with SCD and 50 unrelated normal individuals as controls were enrolled in. Th...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Molecular Vision
2011
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3209473/ https://ncbi.nlm.nih.gov/pubmed/22065921 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|