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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.
Pediatr Hematol Oncol. 2021 Mar;38(2):184-190. doi: 10.1080/08880018.2020.1829219. Epub 2020 Nov 2.
Pediatr Hematol Oncol. 2021.
PMID: 33136529
No abstract available.
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