Detalhe da pesquisa
1.
Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2.
Am J Hum Genet
; 102(3): 505-514, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29499166
2.
Spectrum and frequencies of mutations in the MFN2 gene and its phenotypical expression in Czech hereditary motor and sensory neuropathy type II patients.
Mol Med Rep
; 8(6): 1779-84, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24126688