Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica-Reference-Cited by-同舟云学术

Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica

Published:2020-01-25 Issue:5 Volume:41 Page:906-912
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Vahidnezhad Hassan¹²,Youssefian Leila¹,Sotoudeh Soheila³,Liu Lu⁴,Guy Alyson⁴,Lovell Patricia A.⁴,Kariminejad Ariana⁵,Zeinali Sirous²,McGrath John A.⁶,Uitto Jouni¹^ORCID

Affiliation:

1. Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College and Jefferson Institute of Molecular MedicineThomas Jefferson UniversityPhiladelphia Pennsylvania

2. Molecular Medicine DepartmentBiotechnology Research Center, Pasteur Institute of IranTehran Iran

3. Department of DermatologyChildren's Medical Center, Pediatric Center of Excellence, Tehran University of Medical SciencesTehran Iran

4. Viapath, St. Thomas' HospitalLondon UK

5. Clinical Genetics DeaprtmentKariminejad‐Najmabadi Pathology and Genetics CenterTehran Iran

6. St. John's Institute of DermatologyKing's College London (Guy's Campus)London UK

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.23980

Reference27 articles.

1. Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: emphasizing the role of consanguinity

2. Zinc deficiency and its management in the pediatric population: A literature review and proposed etiologic classification

3. Case 32-2008

4. Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification

5. Blood Vitamin and Trace Metal Levels in Epidermolysis Bullosa

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