{"id":"W4233296897","doi":"10.1097/iop.0b013e3181b59eea","title":"Expanding the Phenotype of a Neurofibromatosis Type 1–Like Syndrome: A Patient With a SPRED1 Mutation and Orbital Manifestations","year":2009,"lang":"en","type":"article","venue":"Ophthalmic Plastic and Reconstructive Surgery","topic":"Neurofibromatosis and Schwannoma Cases","field":"Medicine","cited_by":3,"is_retracted":true,"has_abstract":true,"ca_institutions":"Object Research Systems (Canada)","funders":"Massachusetts General Hospital","keywords":"Medicine; Neurofibromatosis; Dermatology; Pathology; Mutation; Biopsy; Neurofibromatosis type 2; Neurofibromatoses; Genetics; Gene; Biology","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":{"nature":"Retraction","reason":"Error in Data;Error in Results and/or Conclusions;Miscommunication with/by Author;Unreliable Data;Unreliable Results and/or Conclusions;","date":"3/1/2010 0:00","openalex_flagged":true},"screen":null}