Exploring the Molecular Interaction Between NR2E3 and NR1D1 in Retinitis Pigmentosa: A Docking and Molecular Dynamics Study von Vafaeie, Farzane, Mohammadpour, Mojtaba, Etesam, Shokoofeh, Zarifi, Shahnaz, Yari, Abolfazl, Nikandish, Malihe, Hashemzadeh, Hassan, Hajiabadi, Mohammad Reza, Miri-Moghaddam, Ebrahim

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Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation von Shadmehri, Azam Ahmadi, Fattahi, Najmeh, Pourreza, Mohammad Reza, Koohiyan, Mahboobeh, Zarifi, Shahnaz, Darbouy, Mojtaba, Sharifi, Reza, Tavakkoly Bazzaz, Javad, Tabatabaiefar, Mohammad Amin

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Identification of Edward’s Syndrome and the Importance of Maternal SerumScreening Tests von Shahnaz Zarifi, Ashraf Ahmadi Shadmehri, Aazam Ahmadi Shadmehri

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Identification of Edward’s Syndrome and the Importance of Maternal SerumScreening Tests von Zarifi, Shahnaz, Ahmadi Shadmehri, Ashraf, Ahmadi Shadmehri, Aazam

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Identification of the Peroxisomal Biogenesis Factor 1 Gene Point Mutation in an Iranian Family with Zellweger Syndrome (ZS) von Parsamanesh, Negin, Ahmadi Shadmehri, Aazam, Zarifi, Shahnaz, Miri-Moghaddam, Ebrahim

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