Analysis of Corneal Phenotypes in Japanese Patients With Myotonic Dystrophy Type 1
Japanese patients with DM1 without TNR expansion in TCF4 have a mild phenotype equivalent to Fuchs endothelial corneal dystrophy. Endothelial cell density is higher in DM1 patients than in normal participants.
Authors
- Masayuki Nakamori (ORCID: https://orcid.org/0000-0003-4714-3044)
- Tomoya Kubota (ORCID: https://orcid.org/0000-0003-1004-8537)
- Sayo Maeno (ORCID: https://orcid.org/0000-0002-0301-6775)
- Kohji Nishida (ORCID: https://orcid.org/0000-0001-9069-3610)
- Chifune Kai
- Masanori Takahashi (ORCID: https://orcid.org/0000-0002-5513-5012)
- Ryota Koto
- Yoshinori Oie (ORCID: https://orcid.org/0000-0003-2291-800X)
- Nozomi Nishida
- Motokazu Tsujikawa (ORCID: https://orcid.org/0009-0008-1084-7340)
- Kenya Kubo
Institutions
- The University of Osaka (JP)
Publication Details
- Journal
- Cornea
- Published
- 2024-08-21
- DOI
- https://doi.org/10.1097/ico.0000000000003679
- Citations
- 2
- Primary Topic
- Genetic Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.54