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Autor:
Thais Regina Ferreira de Melo, Jean Leandro dos Santos, Lucas dos Reis Ercolin, CarolinaLanaro, Chung Man Chin, Aylime Castanho Bolognesi Melchior, RafaelConsolin Chelucci
Publikováno v:
Inherited Hemoglobin Disorders
Sickle cell disease (SCD) is one of the most common genetic disorders worldwide. It is caused by a point mutation that changes glutamic acid (Glu6) to valine (Val6) in the β chain of hemoglobin. Vaso-occlusion is the most well-known problem associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff101c1e05a7ba58028d44dc880b01b7
https://doi.org/10.5772/60515
https://doi.org/10.5772/60515
