Hypotrichosis simplex of the scalp and peeling skin disease, two sides of the same coin-Reference-Cited by-同舟云学术

Hypotrichosis simplex of the scalp and peeling skin disease, two sides of the same coin

Published:2022-06-07 Issue:10 Volume:36 Page:
ISSN:0926-9959
Container-title:Journal of the European Academy of Dermatology and Venereology
language:en
Short-container-title:Acad Dermatol Venereol

Author:

López‐Balboa P.¹^ORCID,Martos‐Cabrera L.¹^ORCID,Ramírez‐Lluch M.¹^ORCID,Noguera‐Morel L.^ORCID,Ortiz‐Cabrera N. V.²^ORCID,González‐Sarmiento R.³^ORCID,Torrelo A.¹^ORCID,Hernández‐Martín Á.¹^ORCID

Affiliation:

1. Department of Dermatology Hospital Infantil Universitario Niño Jesús Madrid Spain

2. Clinical Genetics Hospital Infantil Universitario Niño Jesús Madrid Spain

3. Molecular Medicine Unit‐Department of Medicine IBSAL and IBMCC and University Hospital of Salamanca, CSIC, University of Salamanca Salamanca Spain

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jdv.18271

Reference10 articles.

1. Evidence for a role of corneodesmosin, a protein which may serve to modify desmosomes during cornification, in stratum corneum cell cohesion and desquamation

2. Hereditary hypotrichosis simplex of the scalp.

3. A Gene for Hypotrichosis Simplex of the Scalp Maps to Chromosome 6p21.3

4. Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

5. A novel insertion mutation of CDSN responsible for hypotrichosis simplex of scalp in a Chinese family

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