Loss of coordinated expression between ribosomal and mitochondrial genes revealed by comprehensive characterization of a large family with a rare Mendelian disorder-Reference-Cited by-同舟云学术

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Loss of coordinated expression between ribosomal and mitochondrial genes revealed by comprehensive characterization of a large family with a rare Mendelian disorder

Published:2021-07 Issue:4 Volume:113 Page:1895-1905
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Panici Brendan,Nakajima Hosei,Carlston Colleen M.,Ozadam Hakan,Cenik Can,Cenik Elif Sarinay

Funder

NIH

Welch Foundation

Cancer Prevention and Research Institute of Texas

University of Texas at Austin

Publisher

Elsevier BV

Subject

Genetics

Reference64 articles.

1. Untangling the phenotypic heterogeneity of Diamond Blackfan anemia;Farrar;Semin. Hematol.,2011

2. Diamond Blackfan anemia 2008-2009: broadening the scope of ribosome biogenesis disorders;Lipton;Curr. Opin. Pediatr.,2010

3. Ribosome levels selectively regulate translation and lineage commitment in human hematopoiesis;Khajuria;Cell,2018

4. Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia;Sankaran;J. Clin. Invest.,2012

5. The genetic landscape of diamond-Blackfan Anemia;Ulirsch;Am. J. Hum. Genet.,2018

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