Detalhe da pesquisa
1.
Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying MME mutations.
J Med Genet
; 55(12): 814-823, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30415211
2.
A very mild phenotype of Charcot-Marie-Tooth disease type 4H caused by two novel mutations in FGD4.
J Neurol Sci
; 402: 156-161, 2019 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31152969