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pro vyhledávání: '"Marion Dornwell"'
Autor:
Arnulf Pekrun, Refik Ozcan, Bernard G. Forget, Marion Dornwell, Patrick G. Gallagher, Jennifer M. Gonzalez, Jutta Herbers, Samuel E. Lux, Marcia L. Lux, Alphonse L. Scarpa, Wilfried Kugler, William T. Tse, Werner Schroter, Stefan W. Eber
Publikováno v:
Nature genetics. 13(2)
Hereditary spherocytosis (HS) is the most common inherited haemolytic anaemia in Northern Europeans. The primary molecular defects reside in the red blood cell (RBC) membrane, particularly in proteins that link the membrane skeleton to the overlying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d377331363300182094ffaadf0472e8f
https://pubmed.ncbi.nlm.nih.gov/8640229
https://pubmed.ncbi.nlm.nih.gov/8640229
