Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma

Detalles Bibliográficos
Autores principales: Goussot, Raphaëlle, Prasad, Megana, Stoetzel, Corinne, Lenormand, Cédric, Dollfus, Hélène, Lipsker, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358901/
https://www.ncbi.nlm.nih.gov/pubmed/28349113
http://dx.doi.org/10.1016/j.jdcr.2017.01.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358901/
https://www.ncbi.nlm.nih.gov/pubmed/28349113
http://dx.doi.org/10.1016/j.jdcr.2017.01.002

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