Search Results - "Molero Magariño, M."

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    PS1204 SEVERE HEREDITARY HAEMOLYTIC ANAEMIA DUE TO THREE NOVEL SPTA1 MUTATIONS IN TWO COMPOUND HETEROZYGOUS UNRELATED PATIENTS by Krishnevskaya, E., Rodriguez, I. Hernandez, Serra, A. Ancochea, Payán‐Pernía, S., Rizzuto, V., Magariño, M. Molero, Vives‐Corrons, J.‐L.

    Published in HemaSphere (01-06-2019)
    “…Background: Red blood cell (RBC) membrane defects are a cause of hereditary haemolytic anaemia (HHA) due to mutations in the genes that encode cytoskeletal…”
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    Journal Article