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Article

FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis.

Gene - 5 Sept 2017

Radha Rama Devi Akella, Panday Nagesh Narayan, Naushad Shaik Mohammad

Abstract excerpt

The Forkhead box N1 (FOXN1) is a transcriptional factor regulating the development, differentiation and function of thymic epithelial cells; maintaining T-lineage progenitors in bone marrow; promoting terminal differentiation of epithelial cells of hair follicles. Mutation in FOXN1 was reported to cause a rare disorder characterized by rudimentary thymus gland, T-cell immunodeficiency, congenital alopecia and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 28636882
DOI: 10.1016/j.gene.2017.06.033

Genes

FOXN1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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