Search Results - Shisseh, Hafsa

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    Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1

    Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1 by Hilal, Latifa, Boutayeb, Soraya, Serrou, Aziza, Refass-Buret, Loubna, Shisseh, Hafsa, Bencherifa, Fatiha, El Mzibri, Mohammed, Benazzouz, Bouchra, Berraho, Amina

    Published in Molecular vision
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