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Scientific reports, ISSN 2045-2322, 11/2018, Volume 8, Issue 1, pp. 17227 - 17227
A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has not been fixed in the paper. 
Journal Article
SEMINARS IN HEMATOLOGY, ISSN 0037-1963, 04/2017, Volume 54, Issue 2, pp. 57 - 59
Journal Article
PLoS Genetics, ISSN 1553-7390, 07/2015, Volume 11, Issue 7
  Mutations in ribosomal protein (RP) genes can result in the loss of erythrocyte progenitor cells and cause severe anemia. This is seen in patients with... 
Bone marrow | Mutation | Genes | Apoptosis
Journal Article
Journal of pediatric hematology/oncology, ISSN 1077-4114, 03/2019, p. 1
Diamond-Blackfan Anemia (DBA) is a rare inherited form of pure red cell aplasia that usually manifests in infancy or early childhood, and is characterized by... 
Journal Article
Blood, ISSN 0006-4971, 03/2016, Volume 127, Issue 11, pp. 1387 - 1397
Journal Article
Blood, ISSN 0006-4971, 10/2012, Volume 120, Issue 15, pp. 3048 - 3057
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2014, Volume 95, Issue 1, pp. 96 - 107
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 03/2017, Volume 100, Issue 3, pp. 506 - 522
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 3090 - 17
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2019, Volume 104, Issue 6, pp. 1040 - 1059
The heterogeneous nuclear ribonucleoprotein ( ) genes code for a set of RNA-binding proteins that function primarily in the spliceosome C complex. Pathogenic... 
microcephaly | neurodevelopment | spliceosome C | brachydactyly | seizures | HNRNPR | homeobox | developmental disorder
Journal Article