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, 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

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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.

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