Detalhe da pesquisa
1.
Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome.
Eur J Immunol
; 50(7): 1078-1080, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32181500