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RPL35A gene

Known as: L35A, RIBOSOMAL PROTEIN L35A, RPL35A 
National Institutes of Health

Related topics

Related topics

1 relation
RPL10L gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Table 2. [Selected RPL35A Pathogenic Variants].
2016
2016
Neurological Deficits of an Rps 19 ( Arg 67 del ) Model of Diamond-Blackfan Anaemia ( Diamond-Blackfan anaemia / RPS 19 / transgenic mouse / gait / neuromuscular function / fear conditioning )
Diamond-Blackfan anaemia is a rare disease caused by insufficient expression of ribosomal proteins and is characterized by… 
2013
2013
Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond–Blackfan anemia
Diamond–Blackfan anemia (DBA) is an inherited red blood cell aplasia that usually presents during the first year of life. The… 
Review
2012
Review
2012
RPS29 is Mutated in a Multi-Case Diamond Blackfan Anemia Family
Abstract 511 Diamond Blackfan anemia (DBA) is an inherited bone marrow failure syndrome (IBMFS) characterized by red blood cell… 
2010
2010
New Determination Method for Extensive Gene Deletions In Diamond–Blackfan Anemia
Abstract 4231 Introduction: Fifty percent of Diamond–Blackfan anemia (DBA) patients possess mutations in ribosomal protein genes… 
2001
2001
Physical and transcript map of the dominant optic atrophy (OPA1) gene critical region at 3q28-q29.
The dominant optic atrophy gene (OPA1) has previously been mapped to chromosome 3q28-q29. We have now constructed a physical and… 
1990
1990
cDNA encoding the human homologue of rat ribosomal protein L35a.
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