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Hereditary red blood cell membrane defects. Detection of PIEZO1 mutations associated with SPTA1 mutations. An unusual clinical case of hereditary xerocytosis.

Pediatric hematology and oncology - 1 Mar 2021

Fortugno Carmelo, Galea Eulalia, Cantaffa Renato, Gigliotti Francesco, Fabiano Rachele Lucia, Talarico Valentina, Raiola Giuseppe, Galati Maria Concetta

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Share to Anemia, Hemolytic, Congenital
Share to Cell Membrane
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Hydrops Fetalis

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Share to Spherocytosis, Hereditary

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Identifiers

PMID: 33136529
DOI: 10.1080/08880018.2020.1829219

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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Hereditary red blood cell membrane defects. Detection of PIEZO1 mutations associated with SPTA1 mutations. An unusual clinical case of hereditary xerocytosis.PMID 33136529Read ↗

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