Detalhe da pesquisa
1.
TPC2 polymorphisms associated with a hair pigmentation phenotype in humans result in gain of channel function by independent mechanisms.
Proc Natl Acad Sci U S A
; 114(41): E8595-E8602, 2017 10 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28923947
2.
Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2.
Hum Mol Genet
; 23(6): 1538-50, 2014 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24163243
3.
Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2.
Hum Mol Genet
; 26(2): 466, 2017 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28365780