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Paper Details

A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT.
Blood
55
2013
8-MB deletion, GPI-anchored protein, GPI-anchored protein deficiency, PIGA, PIGT, PNH, X-chromosomal gene, X-chromosomal gene PIGA, exons, gene PIGT, granulocytes, hematopoietic stem cells, paroxysmal nocturnal hemoglobinuria
Author NameAffiliation
Peter M KrawitzInstitute for Medical Genetics and Human Genetics, Charite Universitatsmedizin
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Datasets

Release 1.2