Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II

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Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders

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SNARE Selectivity of the COPII Coat

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Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking

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The Genetic Basis of a Craniofacial Disease Provides Insight into COPII Coat Assembly

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Secretory COPII coat component Sec23a is essential for craniofacial chondrocyte maturation

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Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts.

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The Transport Signal on Sec22 for Packaging into COPII-Coated Vesicles Is a Conformational Epitope

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Coordination of COPII vesicle trafficking by Sec23

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Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency

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Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation

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Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search

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Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects.

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Erythroid differentiation and maturation from peripheral CD34+ cells in liquid culture: Cellular and molecular characterization

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Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): Where are we now?

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A Systematic Mammalian Genetic Interaction Map Reveals Pathways Underlying Ricin Susceptibility

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Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta

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Ineffective erythropoiesis and regulation of iron status in iron loading anaemias

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SEC24A deficiency lowers plasma cholesterol through reduced PCSK9 secretion

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The ULK1-FBXW5-SEC23B nexus controls autophagy

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