A recessive mutation in the DSP gene linked to cardiomyopathy, skin fragility and hair defects impairs the binding of desmoplakin to epidermal keratins and the muscle-specific intermediate filament desmin.

Favre, Bertrand; Begré, N; Borradori, Luca (2018). A recessive mutation in the DSP gene linked to cardiomyopathy, skin fragility and hair defects impairs the binding of desmoplakin to epidermal keratins and the muscle-specific intermediate filament desmin. British journal of dermatology, 179(3), pp. 797-799. Wiley-Blackwell 10.1111/bjd.16832

[img] Text
Favre_et_al-2018-British_Journal_of_Dermatology.pdf - Published Version
Restricted to registered users only
Available under License Publisher holds Copyright.
Download (289kB)

Item Type:

 Journal Article (Original Article)

Division/Institute:

 04 Faculty of Medicine > Department of Dermatology, Urology, Rheumatology, Nephrology, Osteoporosis (DURN) > Clinic of Dermatology

UniBE Contributor:

 Favre, Bertrand, Borradori, Luca

Subjects:

 600 Technology > 610 Medicine & health

ISSN:

 0007-0963

Publisher:

 Wiley-Blackwell

Language:

 English

Submitter:

 Andrea Studer-Gauch

Date Deposited:

 30 Nov 2018 09:58

Last Modified:

 05 Dec 2022 15:21

Publisher DOI:

 10.1111/bjd.16832

PubMed ID:

 29878302

BORIS DOI:

 10.7892/boris.121872

URI:

 https://boris.unibe.ch/id/eprint/121872

Actions (login required)

Edit item Edit item
Provide Feedback