Brownlie, A., Donovan, A., Pratt, S.J., Paw, B.H., Oates, A.C., Brugnara, C., Witkowska, H.E., Sassa, S., and Zon, L.I. (1998) Positional cloning of the zebrafish sauternes gene: a model for congenital sideroblastic anaemia. Nature Genetics. 20:244-250
|
Crispin, A., Guo, C., Chen, C., Campagna, D.R., Schmidt, P.J., Lichtenstein, D.A., Cao, C., Sendamarai, A.K., Hildick-Smith, G.J., Huston, N.C., Boudreaux, J., Bottomley, S.S., Heeney, M.M., Paw, B.H., Fleming, M.D., Ducamp, S. (2020) Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemia. The Journal of Clinical Investigation. 130(10):5245-5256
|
Fernández-Murray, J.P., Prykhozhij, S.V., Dufay, J.N., Steele, S.L., Gaston, D., Nasrallah, G.K., Coombs, A.J., Liwski, R.S., Fernandez, C.V., Berman, J.N., McMaster, C.R. (2016) Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia. PLoS Genetics. 12:e1005783
|
LeBlanc, M.A., Bettle, A., Berman, J.N., Price, V.E., Pambrun, C., Yu, Z., Tiller, M., McMaster, C.R., Fernandez, C.V. (2016) Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia. Pediatric blood & cancer. 63(7):1307-9
|
Varga, M., Ralbovszki, D., Balogh, E., Hamar, R., Keszthelyi, M., Tory, K. (2018) Zebrafish Models of Rare Hereditary Pediatric Diseases. Diseases (Basel, Switzerland). 6(2)
|