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

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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 and Borradori, Luca

Subjects:

600 Technology > 610 Medicine & health

ISSN:

0007-0963

Publisher:

Wiley-Blackwell

Language:

English

Submitter:

Sandra Nyffenegger

Date Deposited:

30 Nov 2018 09:58

Last Modified:

16 Jul 2019 15:00

Publisher DOI:

10.1111/bjd.16832

PubMed ID:

29878302

BORIS DOI:

10.7892/boris.121872

URI:

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

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