ArticleHaematologica2013
Mutation spectrum in Chinese patients affected by congenital sideroblastic anemia and a search for a genotype-phenotype relationship.
Article in Haematologica, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
11 citing papers in PubMed, 22 citations in OpenAlex.
- Case report: A novel 11-bp deletion in exon 11 causing a frameshift in the C-terminal of theFrontiers in medicine · 2024Article
- Iron Metabolism in the Disorders of Heme Biosynthesis.Metabolites · 2022Review
- Sideroblastic anaemia in a patient with sickle cell disease.BMJ case reports · 2022Article
- SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature.Human mutation · 2021Review
- [New mutation of congenital sideroblastic anemia: a case report and literature review].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2021Review
- [Clinical features and gene mutation spectrum in children with sideroblastic anemia].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2019Article
- Reduced-toxicity allogeneic hematopoietic stem cell transplantation in congenital sideroblastic anemia.Clinical case reports · 2018Article
- [Advances in genes mutation and pathophysiology of congenital sideroblastic anemia].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2016Article
- Sideroblastic anemia: functional study of two novel missense mutations in ALAS2.Molecular genetics & genomic medicine · 2016Article
- Mutation analysis of Chinese sporadic congenital sideroblastic anemia by targeted capture sequencing.Journal of hematology & oncology · 2015Article
- Whole genome sequencing of 35 individuals provides insights into the genetic architecture of Korean population.BMC bioinformatics · 2014Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors at 6 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.