1.
Clin Case Rep
; 8(12): 2976-2985, 2020 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33363863
RESUMO
This investigation facilitates a better understanding of inhibitor development, the critical treatment morbidity in HA patients. Furthermore, six novel mutations are reported, which would expand the mutation spectrum of the F8 gene.