Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency
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Published:2019-08
Issue:
Volume:81
Page:91-106
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ISSN:0945-053X
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Container-title:Matrix Biology
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language:en
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Short-container-title:Matrix Biology
Author:
Vahidnezhad Hassan,
Youssefian Leila,
Saeidian Amir Hossein,
Touati Andrew,
Pajouhanfar Sara,
Baghdadi Taghi,
Shadmehri Azam Ahmadi,
Giunta Cecilia,
Kraenzlin Marius,
Syx Delfien,
Malfait FransiskaORCID,
Has CristinaORCID,
Lwin Su M.,
Karamzadeh Razieh,
Liu Lu,
Guy Alyson,
Hamid Mohammad,
Kariminejad Ariana,
Zeinali Sirous,
McGrath John A.,
Uitto Jouni
Funder
Ghent University
DEBRA International
Subject
Molecular Biology
Cited by
43 articles.
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