Identification of two novel mutations in the cornea-specific TGFBI gene causing unique phenotypes in patients with corneal dystrophies
Crossref DOI link: https://doi.org/10.1007/s10792-016-0216-5
Published Online: 2016-03-10
Published Print: 2016-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Foja, Sabine https://orcid.org/0000-0002-2703-5540
Hoffmann, Katrin
Auw-Haedrich, Claudia
Reinhard, Thomas
Rupprecht, Andreas
Gruenauer-Kloevekorn, Claudia
Text and Data Mining valid from 2016-03-10