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FKBP14-related Ehlers-Danlos syndrome: expansion of the phenotype to include vascular complications.
Murray, Mitzi L; Yang, Margaret; Fauth, Christine; Byers, Peter H.
Affiliation
  • Murray ML; Department of Pathology, University of Washington, Seattle, Washington; Department of Medicine (Medical Genetics), University of Washington, Seattle, Washington.
Am J Med Genet A ; 164A(7): 1750-5, 2014 Jul.
Article in En | MEDLINE | ID: mdl-24677762
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Peptidylprolyl Isomerase / Ehlers-Danlos Syndrome / Genetic Association Studies / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2014 Type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Peptidylprolyl Isomerase / Ehlers-Danlos Syndrome / Genetic Association Studies / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2014 Type: Article