FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference10 articles.
1. Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population;Adriani;Ann. Hum. Genet.,2004
2. FOXN1 homozygous mutation associated with anencephaly and severe neural tube defect in human athymic nude/SCID fetus;Amorosi;Clin. Genet.,2008
3. Brain alteration in a nude/SCID fetus carrying FOXN1 homozygous mutation;Amorosi;J. Neurol. Sci.,2010
4. Nail dystrophy associated with a heterozygous mutation of the nude/SCID human FOXN1 (WHN) gene;Auricchio;Arch. Dermatol.,2005
5. A novel mutation in FOXN1 resulting in SCID: a case report and literature review;Chou;Clin. Immunol.,2014
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2. Thymic Development, Inborn Errors of Immunity with Thymic Dysfunction and Thymic Transplantation;Asthma Allergy Immunology;2023-08
3. Eyebrow and Eyelash Alopecia: A Clinical Review;American Journal of Clinical Dermatology;2022-10-02
4. Novel heterozygous FOXN1 mutation identified following newborn screening for severe combined immunodeficiency is associated with improving immune parameters;LymphoSign Journal;2022-06-01
5. T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy;Genetic Syndromes;2022
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