Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with a SPRED1 mutation and orbital manifestations.

Lane KA, Anninger WV, Katowitz JA

Open source

DOI
10.1097/iop.0b013e3181b59eea
Published
2009 Sep-Oct
Container
Ophthalmic plastic and reconstructive surgery
Publisher
Not recorded
Open access
unknown

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BibTeX

@article{allodium:10.1097/iop.0b013e3181b59eea,
  title = {Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with a SPRED1 mutation and orbital manifestations.},
  author = {Lane KA and Anninger WV and Katowitz JA},
  year = {2009},
  journal = {Ophthalmic plastic and reconstructive surgery},
  doi = {10.1097/iop.0b013e3181b59eea},
  url = {https://doi.org/10.1097/iop.0b013e3181b59eea}
}

RIS

TY  - JOUR
TI  - Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with a SPRED1 mutation and orbital manifestations.
AU  - Lane KA
AU  - Anninger WV
AU  - Katowitz JA
PY  - 2009
JO  - Ophthalmic plastic and reconstructive surgery
DO  - 10.1097/iop.0b013e3181b59eea
UR  - https://doi.org/10.1097/iop.0b013e3181b59eea
ER  - 

APA

KA, L., WV, A., & JA, K. (2009). Expanding the phenotype of a neurofibromatosis type 1-like syndrome: a patient with a SPRED1 mutation and orbital manifestations.. Ophthalmic plastic and reconstructive surgery. https://doi.org/10.1097/iop.0b013e3181b59eea

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