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...

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Detalles Bibliográficos
Autores principales: Bushehri, Ata, Zare-Abdollahi, Davood, Alavi, Afagh, Dehghani, Alireza, Mousavimikala, Mohammadreza, Khorram Khorshid, Hamid Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2019
Materias:
Original Article
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

Internet

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

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