Showing 1 - 3 results of 3 for search 'Samin sharafian', query time: 0.06s
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JAGN1 mutation with distinct clinical features; two case reports and literature review by Mahsa Hojabri, Yeganeh Farsi, Mahnaz Jamee, Hassan Abolhassani, Hedieh Haji Khodaverdi Khani, Abdollah Karimi, Mehrnaz Mesdaghi, Zahra Chavoshzadeh, Samin Sharafian
Published 2023Connect to this object online.
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