Genotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathy
Erişim
info:eu-repo/semantics/closedAccessTarih
2021Yazar
Acarli, Ayse OzdagCakar, Arman
Candayan, Ayse
Durmus, Hacer
Ceylaner, Serdar
Matur, Zeliha
Oge, Ali
Üst veri
Tüm öğe kaydını gösterÖzet
[No Abstract Available] 427