Search Results - Rafat Ahmed

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    Hereditary spherocytosis due to a novel variant, p.Q1034X, in the beta subunit of the spectrin gene: A case report by Emmalee M. Kugler, Akash Patel, Faraz Afridi, Maria I. Scarano, Rafat Ahmed

    Published 2024
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    Spherocytosis in Newborn Secondary to Novel Heterozygous Mutation in Gene: Case Report by Daphna Varadi MD, Benjamin Caplan MD, Maria Scarano PhD, Rafat Ahmed MD

    Published 2023
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