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Geographical Variability in CYP1B1 Mutations in Primary Congenital Glaucoma
Primary congenital glaucoma (PCG) is a rare type of glaucoma that is inherited in an autosomal recessive manner. PCG can lead to blindness if not detected early in children aged 3 or younger. PCG varies in presentation among various populations, where disease presentation and disease severity vary b...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999900/ https://www.ncbi.nlm.nih.gov/pubmed/35407656 http://dx.doi.org/10.3390/jcm11072048 |