Disruption of Slc52a3 gene causes neonatal lethality with riboflavin deficiency in mice

بواسطة Yoshimatsu, Hiroki, Yonezawa, Atsushi, Yamanishi, Kaori, Yao, Yoshiaki, Sugano, Kumiko, Nakagawa, Shunsaku, Imai, Satoshi, Omura, Tomohiro, Nakagawa, Takayuki, Yano, Ikuko, Masuda, Satohiro, Inui, Ken-ichi, Matsubara, Kazuo
الحاوية / القاعدة Sci Rep (2016)

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

بواسطة Foley, A. Reghan, Menezes, Manoj P., Pandraud, Amelie, Gonzalez, Michael A., Al-Odaib, Ahmad, Abrams, Alexander J., Sugano, Kumiko, Yonezawa, Atsushi, Manzur, Adnan Y., Burns, Joshua, Hughes, Imelda, McCullagh, B. Gary, Jungbluth, Heinz, Lim, Ming J., Lin, Jean-Pierre, Megarbane, Andre, Urtizberea, J. Andoni, Shah, Ayaz H., Antony, Jayne, Webster, Richard, Broomfield, Alexander, Ng, Joanne, Mathew, Ann A., O’Byrne, James J., Forman, Eva, Scoto, Mariacristina, Prasad, Manish, O’Brien, Katherine, Olpin, Simon, Oppenheim, Marcus, Hargreaves, Iain, Land, John M., Wang, Min X., Carpenter, Kevin, Horvath, Rita, Straub, Volker, Lek, Monkol, Gold, Wendy, Farrell, Michael O., Brandner, Sebastian, Phadke, Rahul, Matsubara, Kazuo, McGarvey, Michael L., Scherer, Steven S., Baxter, Peter S., King, Mary D., Clayton, Peter, Rahman, Shamima, Reilly, Mary M., Ouvrier, Robert A., Christodoulou, John, Züchner, Stephan, Muntoni, Francesco, Houlden, Henry
منشور في 2014