Basan syndrome in a family from South India: a novel SMARCAD1 variant

Clin Exp Dermatol. 2024 Mar 21;49(4):437-440. doi: 10.1093/ced/llad393.

Authors

Irene Mathews^{1

2}, Shivangi Wagh³, Aimin Baby¹, Laxmisha Chandrashekar¹, Ashwin Dalal³

Affiliations

¹ Department of Dermatology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
² Department of Dermatology, AIIMS, Patna, India.
³ Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, Telangana, India.

PMID: 37966719
DOI: 10.1093/ced/llad393

No abstract available

MeSH terms

DNA Helicases
Ectodermal Dysplasia*
Humans
India
Nails, Malformed*

Substances

SMARCAD1 protein, human
DNA Helicases

Supplementary concepts

Basan syndrome