Chargement en cours...
Two novel mutations identified in two Chinese gelatinous drop-like corneal dystrophy families
PURPOSE: To identify the genetic defect in the TACSTD2 gene that causes gelatinous drop-like corneal dystrophy (GDLD) in two unrelated consanguineous Chinese families. METHODS: Genomic DNA was prepared from leukocytes of peripheral venous blood. The coding region of the TACSTD2 gene was evaluated by...
Enregistré dans:
| Auteurs principaux: | , , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Molecular Vision
2007
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2774463/ https://ncbi.nlm.nih.gov/pubmed/17653040 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|