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Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation.

Pediatric blood & cancer - 1 Aug 2023

Munaretto Vania, Martella Maddalena, Francescato Samuela, Reggiani Giulia, Boaro Maria Paola, Bianchi Paola, Fermo Elisa, Barcellini Wilma, Sainati Laura, Colombatti Raffaella

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Share to Anemia, Hemolytic
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 37132095
DOI: 10.1002/pbc.30325

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation.PMID 37132095Read ↗

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