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Novel mutations in LTBP2 identified in familial cases of primary congenital glaucoma
PURPOSE: Primary congenital glaucoma (PCG) is a genetically heterogeneous disorder caused by developmental defects in the anterior chamber and trabecular meshwork. This disease is an important cause of childhood blindness. In this study, we aim to identify the genetic determinants of PCG in three co...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Mol Vis |
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| Κύριοι συγγραφείς: | , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Molecular Vision
2020
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7043638/ https://ncbi.nlm.nih.gov/pubmed/32165823 |
| Ετικέτες: |
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