Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis.

Autor: da Silva-Batista JA; Federal University of Vale do São Francisco, Petrolina, Pernambuco, Brazil. jemimaaraujods@gmail.com., Marques W Jr; School of Medicine of Ribeirão Preto, São Paulo State University, São Paulo, Brazil., Oliveira MTJS; State University of Santa Cruz, Ilheus, Bahia, Brazil., Lins LVC; Bahiana School of Medicine and Public Health, Salvador, Bahia, Brazil., Galvão AJP; Bahia Hospital, Salvador, Bahia, Brazil., Miguel DSCG; Bahiana School of Medicine and Public Health, Salvador, Bahia, Brazil., Machado-Costa MC; Bahiana School of Medicine and Public Health, Salvador, Bahia, Brazil.

Publikováno v: Journal of human genetics [J Hum Genet] 2020 Aug; Vol. 65 (8), pp. 711-713. Date of Electronic Publication: 2020 Apr 09.