Amanote Research
Register
Sign In
Mutation in FAM111B Causes Hereditary Fibrosing Poikiloderma With Tendon Contracture, Myopathy, and Pulmonary Fibrosis
Acta Dermato-Venereologica
- Sweden
doi 10.2340/00015555-3186
Full Text
Open PDF
Abstract
Available in
full text
Categories
Dermatology
Medicine
Date
January 1, 2019
Authors
F Chen
L Zheng
Y Li
H Li
Z Yao
M Li
Publisher
Acta Dermato-Venereologica
Related search
Hereditary Transmission of Dupuytren's Contracture
BMJ
Beyond Idiopathic Pulmonary Fibrosis: The World of Progressive-Fibrosing Interstitial Lung Disease
European Respiratory Review
Pulmonary
Respiratory Medicine
Pulmonary Fibrosis Associated With TINF2 Gene Mutation: Is Somatic Reversion Required?
European Respiratory Journal
Medicine
Pulmonary
Respiratory Medicine
Deranged Fatty Acid Composition Causes Pulmonary Fibrosis in Elovl6-Deficient Mice
Nature Communications
Astronomy
Genetics
Molecular Biology
Biochemistry
Chemistry
Physics
Detection of Anti-Cytokeratin 8 Antibody in the Serum of Patients With Cryptogenic Fibrosing Alveolitis and Pulmonary Fibrosis Associated With Collagen Vascular Disorders
Thorax
Pulmonary
Respiratory Medicine
The Epidemiology of Idiopathic Pulmonary Fibrosis and Interstitial Lung Diseases at Risk of a Progressive-Fibrosing Phenotype
European Respiratory Review
Pulmonary
Respiratory Medicine
GNE Myopathy in Turkish Sisters With a Novel Homozygous Mutation
Case Reports in Neurological Medicine
Prognosis of Combined Pulmonary Fibrosis and Emphysema: Comparison With Idiopathic Pulmonary Fibrosis Alone
Therapeutic Advances in Respiratory Disease
Pulmonary
Respiratory Medicine
Pharmacology
Image Gallery: Poikiloderma With Neutropenia
British Journal of Dermatology
Dermatology
Medicine