Detalhe da pesquisa
1.
The novel p.Ser263Phe mutation in the human high-affinity choline transporter 1 (CHT1/SLC5A7) causes a lethal form of fetal akinesia syndrome.
Hum Mutat
; 40(10): 1676-1683, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31299140