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    Exome sequencing reveals a homozygous frameshift variant in CAPN3 in a Tunisian patient with a neuromuscular disorder

    DOI Logo 10.17352/amgm.000010

    Published On: September 27, 2022 | Pages: 001 - 004

    Author(s): Exome sequencing reveals a homozygous frameshift variant in CAPN3 in a Tunisian patient with a neuromuscular disorder
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    Contribution to the anthropogenetic study by the blood systems of the arabophone population of Beni Mellal Area

    Author(s): Ossmani HE
    Received Date: 29 Dec, 2020

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