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Description
Mikolic A, Karaconji IB
The most common approach is to employ specific inhibitors to dissect/hinder the function of gB, gH, and gD in the entry process [117]
Available at: Lafuente, Rafael & Gonzlez-Comadrn, Mireia & Sol, Ivan & Granollers, Gemma & Brassesco, Mario & Carreras, Ramn & Checa, Miguel
10.1097/01.tp.0000178305.39231.a2 [DOI] [PubMed] [Google Scholar] Foss C
Nezu J, Tamai I, Oku A, Ohashi R, Yabuuchi H, Hashimoto N, Nikaido H, Sai Y, Koizumi A, Shoji Y, Takada G, Matsuishi T, Yoshino M, Kato H, Ohura T, Tsujimoto G, Hayakawa J, Shimane M, Tsuji A: Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
