Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome.
Colobran, Roger; Álvarez de la Campa, Elena; Soler-Palacín, Pere; Martín-Nalda, Andrea; Pujol-Borrell, Ricardo; de la Cruz, Xavier; Martínez-Gallo, Mónica.
; 163: 60-5, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26748374
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