LymphedemaV1, France, Analysis, bibRecord, 000019

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

Identifieur interne : 000019 ( France/Analysis ); précédent : 000018; suivant : 000020

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

Auteurs : Raphaëlle Goussot [France] ; Megana Prasad [France] ; Corinne Stoetzel [France] ; Cédric Lenormand [France] ; Hélène Dollfus [France] ; Dan Lipsker [France]

Source :

JAAD Case Reports [ 2352-5126 ] ; 2017.

RBID : PMC:5358901
Url:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358901

DOI: 10.1016/j.jdcr.2017.01.002
PubMed: 28349113
PubMed Central: 5358901

Affiliations:

Links to Exploration step

PMC:5358901

Le document en format XML

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   |texte=   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
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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

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

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