TrianglePUBLICATIONS · 24523240
Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis.
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Bibliographic metadata only. No full-text article or abstract is reproduced. Absence of a captured notice is not confirmation that a publication is clear of corrections or retractions.
- Journal
- Blood
- Publication date
- 2014 Apr 3
- First author
- Skokowa J
Publication notices
- absence is not clearance
- true
- has correction metadata
- false
- has expression of concern metadata
- false
- has retraction in link
- false
- pubmed marks article retracted
- false
- pubmed marks retraction notice
- false
- relationships
Authors and identifiers
- name
- Skokowa J
- type
- Author
- name
- Steinemann D
- type
- Author
- name
- Katsman-Kuipers JE
- type
- Author
- name
- Zeidler C
- type
- Author
- name
- Klimenkova O
- type
- Author
- name
- Klimiankou M
- type
- Author
- name
- Unalan M
- type
- Author
- name
- Kandabarau S
- type
- Author
- name
- Makaryan V
- type
- Author
- name
- Beekman R
- type
- Author
- name
- Behrens K
- type
- Author
- name
- Stocking C
- type
- Author
Complete bibliographic record and source provenance
- authors
- name
- Skokowa J
- type
- Author
- name
- Steinemann D
- type
- Author
- name
- Katsman-Kuipers JE
- type
- Author
- name
- Zeidler C
- type
- Author
- name
- Klimenkova O
- type
- Author
- name
- Klimiankou M
- type
- Author
- name
- Unalan M
- type
- Author
- name
- Kandabarau S
- type
- Author
- name
- Makaryan V
- type
- Author
- name
- Beekman R
- type
- Author
- name
- Behrens K
- type
- Author
- name
- Stocking C
- type
- Author
- bibliography ids
- nci-bib-3a289708dad8086d4a0fc281
- book metadata
- content sha256
- fc68ba41141b8ce7df99ee4e3dce63d3918d1b6d51b02e63e191481f5cb6298c
- document type
- citation
- dois
- 10.1182/blood-2013-11-538025
- electronic publication date
- display
- 2014 Feb 12
- precision
- day
- year
- 2014
- evidence scope
- bibliographic_metadata_only
- id
- pubmed:24523240
- immutable id
- pubmed:24523240@fc68ba41141b8ce7df99ee4e3dce63d3918d1b6d51b02e63e191481f5cb6298c
- journal
- abbreviation
- Blood
- issn electronic
- 1528-0020
- issn print
- 0006-4971
- issue
- 14
- name
- Blood
- nlm unique id
- 7603509
- pages
- 2229-37
- volume
- 123
- languages
- eng
- notices
- absence is not clearance
- true
- has correction metadata
- false
- has expression of concern metadata
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- has retraction in link
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- pubmed marks article retracted
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- pubmed marks retraction notice
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- relationships
- outcomes validated
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- pmid
- 24523240
- provenance
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- af10498814d931b53231
- provider
- NCBI PubMed ESummary
- record sha256
- f4fefe6ac9fbe425dc78b41a19ca2d4770d914f20c1b0477de8d2067e6bdcd01
- response sha256
- 077a09272afe77e74d5ff01cb33335ddb8a638b7afbafb70ec20e837a0c85c7f
- retrieved at
- 2026-09-09T23:47:00.193465+00:00
- publication date
- display
- 2014 Apr 3
- precision
- day
- year
- 2014
- publication types
- Journal Article
- Research Support, Non-U.S. Gov't
- record status
- PubMed - indexed for MEDLINE
- schema version
- 1.0
- title
- Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis.
Preserved source evidence · Independent clinical review pending · Not medical advice