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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Vydáno v:Int J Mol Cell Med
Hlavní autoři: Bushehri, Ata, Zare-Abdollahi, Davood, Alavi, Afagh, Dehghani, Alireza, Mousavimikala, Mohammadreza, Khorram Khorshid, Hamid Reza
Médium: Artigo
Jazyk:Inglês
Vydáno: Babol University of Medical Sciences 2019
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7241841/
https://ncbi.nlm.nih.gov/pubmed/32489947
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22088/IJMCM.BUMS.8.3.179
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