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Published in 2022 at "Frontiers in Pediatrics"
DOI: 10.3389/fped.2022.796149
Abstract: Background Primary erythrocytic (PEM) is a rare autosomal dominant single gene disease. Most of the changes of gene loci can be found by whole exon gene sequencing, and the clinical symptoms and patient survival can…
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Keywords:
erythromelalgia mainly;
primary erythromelalgia;
crisis;
hypertensive crisis ... See more keywords