Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene: A simple diagnostic approach

International Journal of Laboratory Hematology

Volumn 36, Issue 4, 2014, Pages

  Sandberg, M B ^a   Nybo, M ^a   Birgens, H ^b   Frederiksen, H ^a,c  

^a ODENSE UNIVERSITY HOSPITAL   (Denmark)

^b GENTOFTE UNIVERSITY HOSPITAL   (Denmark)

^c AARHUS UNIVERSITY HOSPITAL   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN; POTASSIUM ION; ION CHANNEL; MONOVALENT CATION; PIEZO1 PROTEIN, HUMAN; POTASSIUM; SODIUM;

BONE MARROW BIOPSY; CHROMOSOME 16; CONFOCAL MICROSCOPY; FAMILIAL HEMOLYSIS; HEMOGLOBIN BLOOD LEVEL; HEMOLYSIS; HYPERBILIRUBINEMIA; HYPERKALEMIA; LETTER; MISSENSE MUTATION; POINT MUTATION; PRIORITY JOURNAL; RETICULOCYTE; SEQUENCE ANALYSIS; SODIUM TRANSPORT; STOMATOCYTOSIS; XEROCYTOSIS; ADULT; ANEMIA, HEMOLYTIC, CONGENITAL; CASE REPORT; ERYTHROCYTE; FEMALE; GENETICS; HUMAN; HYDROPS FETALIS; ION TRANSPORT; MALE; METABOLISM; MIDDLE AGED; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE;

ADULT; ANEMIA, HEMOLYTIC, CONGENITAL; BASE SEQUENCE; CATIONS, MONOVALENT; ERYTHROCYTES; FEMALE; HEMOLYSIS; HUMANS; HYDROPS FETALIS; ION CHANNELS; ION TRANSPORT; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; POTASSIUM; SODIUM;

EID: 84904396735     PISSN: 17515521     EISSN: 1751553X     Source Type: Journal    
DOI: 10.1111/ijlh.12172     Document Type: Letter

References (10)

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