Hasil Pencarian - Hind Almaghthawi

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  1. 1
    Epileptic encephalopathy caused by biallelic mutation in PPM1D: a case report

    Epileptic encephalopathy caused by biallelic mutation in PPM1D: a case report oleh Hind AlMaghthawi, Marwan Nashabat, Majid Alfadhel

    Diterbitkan 2018-06-01
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  2. 2
    HMG-CoA Lyase Deficiency: A Retrospective Study of 62 Saudi Patients

    HMG-CoA Lyase Deficiency: A Retrospective Study of 62 Saudi Patients oleh Majid Alfadhel, Majid Alfadhel, Basma Abadel, Hind Almaghthawi, Muhammad Umair, Zuhair Rahbeeni, Eissa Faqeih, Mohammed Almannai, Ali Alasmari, Mohammed Saleh, Wafaa Eyaid, Wafaa Eyaid, Ahmed Alfares, Ahmed Alfares, Fuad Al Mutairi, Fuad Al Mutairi

    Diterbitkan 2022-05-01
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