Pigmentary anomalies and neurologic symptoms in two siblings-Reference-Cited by-同舟云学术

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Pigmentary anomalies and neurologic symptoms in two siblings

Published:2021-03 Issue:2 Volume:38 Page:
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

Sanke Sarita¹^ORCID, Himadri¹^ORCID,Yadav Jyoti¹,Sharma Suvasini²,Kono Michihiro³⁴,Chander Ram¹

Affiliation:

1. Department of Dermatology and STD Lady Hardinge Medical College New Delhi India

2. Department of Paediatrics Neurology Division Lady Hardinge Medical College New Delhi India

3. Department of Dermatology Nagoya University Graduate School of Medicine Showa‐ku, Nagoya Japan

4. Department of Dermatology and Plastic Surgery Akita University Graduate School of Medicine Akita Japan

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.14469

Reference10 articles.

1. 1000 Genomes Browser [Internet].https://www.ncbi.nlm.nih.gov/variation/tools/1000genomes/help/. Accessed October 22 2020.

2. Dyschromatosis symmetrica hereditaria

3. Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report;Patrizi A;Acta Derm Venereol,1994

4. Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family withADAR1 mutation

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