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Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature.

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Bibliographic Details
Title: Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature.
Authors: Fallahi, Mazdak1 (AUTHOR), Jamee, Mahnaz2 (AUTHOR) mahnaz.jamee@gmail.com, Enayat, Javad1 (AUTHOR), Abdollahimajd, Fahimeh3,4 (AUTHOR), Mesdaghi, Mehrnaz1 (AUTHOR), Khoddami, Maliheh5 (AUTHOR), Segarra-Roca, Anna6,7 (AUTHOR), Frohne, Alexandra6,7 (AUTHOR), Dmytrus, Jasmin6,7 (AUTHOR), Keramatipour, Mohammad8 (AUTHOR), Mansouri, Mahboubeh1 (AUTHOR), Eslamian, Golnaz1 (AUTHOR), Fallah, Shahrzad1 (AUTHOR), Boztug, Kaan6,8,9,10,11 (AUTHOR), Chavoshzadeh, Zahra1 (AUTHOR) zahra_chavoshzadeh@yahoo.com
Source: Allergy, Asthma & Clinical Immunology. 12/24/2022, Vol. 18 Issue 1, p1-9. 9p.
Database: Academic Search Ultimate
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Description
ISSN:17101484
DOI:10.1186/s13223-022-00749-0