Published in
Elsevier, Matrix Biology, (81), p. 91-106, 2019
DOI: 10.1016/j.matbio.2018.11.006
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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
Journal article published in 2019 by
Hassan Vahidnezhad,
Leila Youssefian,
Amir Hossein Saeidian,
Andrew Touati,
Sara Pajouhanfar,
Taghi Baghdadi,
Azam Ahmadi Shadmehri,
Cecilia Giunta,
Marius Kraenzlin,
Delfien Syx,
Fransiska Malfait 
,
Cristina Has ,
Su M. Lwin,
Razieh Karamzadeh,
Lu Liu
and other authors.
,
Cristina Has ,
Su M. Lwin,
Razieh Karamzadeh,
Lu Liu
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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