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Pancreatic SEC23B deficiency is sufficient to explain the perinatal lethality of germline SEC23B deficiency in mice

In humans, loss of function mutations in SEC23B result in Congenital Dyserythropoietic Anemia type II (CDAII), a disease limited to defective erythroid development. Patients with two nonsense SEC23B mutations have not been reported, suggesting that complete SEC23B deficiency might be lethal. We prev...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Khoriaty, Rami, Everett, Lesley, Chase, Jennifer, Zhu, Guojing, Hoenerhoff, Mark, McKnight, Brooke, Vasievich, Matthew P., Zhang, Bin, Tomberg, Kärt, Williams, John, Maillard, Ivan, Ginsburg, David
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4906273/
https://ncbi.nlm.nih.gov/pubmed/27297878
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep27802
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