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Details for article 7 of 9 found articles
| Title: |
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 |
| Author: |
Vahidnezhad, Hassan Youssefian, Leila Saeidian, Amir Hossein Touati, Andrew Pajouhanfar, Sara Baghdadi, Taghi Shadmehri, Azam Ahmadi Giunta, Cecilia Kraenzlin, Marius Syx, Delfien Malfait, Fransiska Has, Cristina Lwin, Su M. Karamzadeh, Razieh Liu, Lu Guy, Alyson Hamid, Mohammad Kariminejad, Ariana Zeinali, Sirous McGrath, John A. Uitto, Jouni |
| Appeared in: |
Matrix biology |
| Paging: | Volume 81 (2019) nr. C pages 91-106 |
| Year: |
2019 |
| Contents: | |
| Publisher: |
Elsevier B.V. |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 7 of 9 found articles
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