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CUGC for posterior polymorphous corneal dystrophy (PPCD)
Name of the disease (synonyms) CUGC for posterior polymorphous corneal dystrophy (PPCD). OMIM# of the disease 122000; 609141; 618031. Name of the analysed genes or DNA/chromosome segments OVOL2 (PPCD1); ZEB1 (PPCD3); GRHL2 (PPCD4). OMIM# of the gene(s) 616441; 189909; 608576. Review of the analytica...
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| Publicat a: | Eur J Hum Genet |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer International Publishing
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6906511/ https://ncbi.nlm.nih.gov/pubmed/31201376 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-019-0448-8 |
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