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Efficient correction of hemoglobinopathy-causing mutations by homologous recombination in integratio...

Efficient correction of hemoglobinopathy-causing mutations by homologous recombination in integratio...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3357996

Efficient correction of hemoglobinopathy-causing mutations by homologous recombination in integration-free patient iPSCs

About this item

Full title

Efficient correction of hemoglobinopathy-causing mutations by homologous recombination in integration-free patient iPSCs

Publisher

London: Nature Publishing Group UK

Journal title

Cell research, 2011-12, Vol.21 (12), p.1740-1744

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Hemoglobinopathies are a collection of heritable diseases caused by abnormal structure or insufficient production of hemoglobins [1]. Many forms of hemo- globinopathies, such as sickle cell disease (SCD) and β-thalassemia, which are caused by mutations of the β-globin (HBB) gene, lead to severe anemia and other life-threatening conditions. Ultimate...

Alternative Titles

Full title

Efficient correction of hemoglobinopathy-causing mutations by homologous recombination in integration-free patient iPSCs

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3357996

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3357996

Other Identifiers

ISSN

1001-0602

E-ISSN

1748-7838

DOI

10.1038/cr.2011.186

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