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Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa
Homozygous mutations of PROS1, encoding vitamin K-dependent protein S (PS), have been reported so far to be associated with purpura fulminans, a characteristic fatal venous thromboembolic disorder. The current work for the first time reports the clinical phenotype in patients with juvenile retinitis...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Babol University of Medical Sciences
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241841/ https://www.ncbi.nlm.nih.gov/pubmed/32489947 http://dx.doi.org/10.22088/IJMCM.BUMS.8.3.179 |