A Novel Arg120Pro Mutation in the RP2 Gene in an Iranian Family with X-linked Retinitis Pigmentosa: A Case Report
As the most common type of inherited retinal degenerative disease, retinitis pigmentosa (RP) has taken clinical and prenatal attention. Considering the clinical importance of consanguineous marriages, new mutations in this type of pregnancy have a high risk and increase the importance of Prenatal Di...
Gorde:
| Egile Nagusiak: | , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Shiraz University of Medical Sciences
2023-11-01
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| Saila: | Iranian Journal of Medical Sciences |
| Gaiak: | |
| Sarrera elektronikoa: | https://ijms.sums.ac.ir/article_49284_be79baa2bbed2c407b74137ad6152c43.pdf |
| Etiketak: |
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