Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with SPRED1 mutation and orbital manifestations: retraction.
Publication/Presentation Date
1-1-2010
Volume
26
Issue
2
First Page
145
Last Page
145
ISSN
1537-2677
Published In/Presented At
Lane, K. A., Anninger, W. V., & Katowitz, J. A. (2010). Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with SPRED1 mutation and orbital manifestations: retraction. Ophthalmic plastic and reconstructive surgery, 26(2), 145. https://doi.org/10.1097/IOP.0b013e3181da5107
Disciplines
Medicine and Health Sciences | Pediatrics
PubMedID
20305530
Department(s)
Department of Pediatrics
Document Type
Article
COinS