Search Results - Mefoung, Samuel Ephrata

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  1. 1
    Case report: Novel variants cause developmental and epileptic encephalopathy in three unrelated families from Mali

    Case report: Novel variants cause developmental and epileptic encephalopathy in three unrelated families from Mali by Bamba, Salia, Sidibé, Lala, Diallo, Seybou H, Cissé, Lassana, Dembélé, Kékouta, Yalcouyé, Abdoulaye, Ji, Weizhen, Dembélé, Mohamed Emile, Diarra, Salimata, Maiga, Alassane Dit Baneye, Traoré, Oumou, Diallo, Salimata, Mefoung, Samuel Ephrata, Touré, Amadou, Koné, Adama, Jeffries, Lauren, Guinto, Cheick O, Mis, Emily K, Fischbeck, Kenneth H, Khokha, Mustafa K, Lakhani, Saquib A, Landouré, Guida

    Published in Frontiers in genetics
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  2. 2
    Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8

    Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8 by Yeetong, Patra, Dembélé, Mohamed E., Pongpanich, Monnat, Cissé, Lassana, Srichomthong, Chalurmpon, Maiga, Alassane B., Dembélé, Kékouta, Assawapitaksakul, Adjima, Bamba, Salia, Yalcouyé, Abdoulaye, Diarra, Salimata, Mefoung, Samuel Ephrata, Rakwongkhachon, Supphakorn, Traoré, Oumou, Tongkobpetch, Siraprapa, Fischbeck, Kenneth H., Gahl, William A., Guinto, Cheick O., Shotelersuk, Vorasuk, Landouré, Guida

    Published in Movement disorders
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