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Confirmation of association of TGFBI p.Ser591Phe mutation with variant lattice corneal dystrophy
- Source :
- Ophthalmic Genetics. 43:530-533
- Publication Year :
- 2022
- Publisher :
- Informa UK Limited, 2022.
- Subjects :
- Ophthalmology
Pediatrics, Perinatology and Child Health
Genetics (clinical)
Subjects
Details
- ISSN :
- 17445094 and 13816810
- Volume :
- 43
- Database :
- OpenAIRE
- Journal :
- Ophthalmic Genetics
- Accession number :
- edsair.doi...........b3e9747eb53495fd2949c0ea85867ad9
- Full Text :
- https://doi.org/10.1080/13816810.2022.2050766