Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2-p13.12/13 deletion

Autor:	Kirsten van Lom, Cornelis L. Harteveld, Ileana Cantú, Rianne Schaap, Sjaak Philipsen, Abdelhafid Natiq, Bella Banjanin, Nynke Gillemans, Abdelaziz Sefiani, Saaid Amzazi, Siham Chafai Elalaoui, Philippe A. Lysy
Přispěvatelé:	Cell biology, Hematology
Rok vydání:	2017
Předmět:	0301 basic medicine Genetics 03 medical and health sciences 030104 developmental biology Hereditary persistence of fetal hemoglobin Cancer research medicine KLF1 Gamma globulin Hematology Biology medicine.disease Haploinsufficiency
Zdroj:	American Journal of Hematology, 92(1), E2-E3. Wiley-Liss Inc. American Journal of Hematology, 92(1), E2-E3
ISSN:	0361-8609
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac277a1810549759ef463109ca4f48f5 https://pure.eur.nl/en/publications/ba8db83e-8f52-4b1e-b58c-af96dd1bc4e0 Zobrazit plný text záznamu Plný text