檢索結果 - Sayed AG

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    Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 10 (LGMD,10), Caused by a Novel Homozygous Variant in the TTN Gene 由 Alghamdi OA, Obaid O, Sayed AG, Farhan H, Sayed J

    出版 2025-06-01
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    Homozygous α-Spectrin (SPTA1) Variant Causing Persistent Hereditary Pyropoikilocytosis in a Newborn: A Case Report and Literature Review 由 Sayed J, Alabdulhadi AS, Alzahrani WA, Joueidi F, Alzahrani GA, Sayed AG, Ebid GT

    出版 2025-10-01
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