Retraction
Expanding the phenotype of a neuroFibromatosis Type 1-like Syndrome: A Patient with SPRED1 Mutation and Orbital Manifestations
Paper Information
Record ID:
2775
Author(s):
Publication Date:
September 01, 2009
Retraction Date:
March 01, 2010
(15.7 years years ago)
Subjects:
Specific Fields:
Biology - Cellular Biology - Molecular Genetics Medicine - Neurology Medicine - Surgery
Biology - Cellular Biology - Molecular Genetics Medicine - Neurology Medicine - Surgery
Institution:
Children’s Hospital of Philadelphia, University of Pennsylvania Hospital System, Philadelphia, Pennsylvania, U.S.ACountry:
🇺🇸 United StatesArticle Type:
Publisher:
Wolters Kluwer
Open Access:
Yes
PubMed ID:
Retraction PubMed ID:
Retraction Details
Retraction Reasons:
Nature of Retraction:
Retraction
Retraction Notice:
10.1097/IOP.0b013e3181da5107Citations (1)
1
Total Citations0
Post-Retraction0
Pre-Retraction1
Same DayPaper citing Expanding the phenotype of a neuroFibromatosis Typ...
Unknown Authors
Unknown Journal
Published: Mar 2010
Same day as retraction
Quick Stats
Total Citations:
1
Years Since Retraction:
15.7 years
Open Access:
Yes
Last Checked:
Never