Autosomal recessive bestrophinopathy combined with neurofibromatosis type 1 in a patient
Abstract Background Neurofibromatosis type 1 (NF1) is a multisystem genetic disorder that may affect multiple systems of the body. Autosomal recessive bestrophinopathy (ARB) is a rare retinal dystrophy caused by autosomal recessively mutations in bestrophin 1 (BEST1) gene. So far, we have not retrie...
Kaydedildi:
| Asıl Yazarlar: | , , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMC
2023-04-01
|
| Seri Bilgileri: | BMC Ophthalmology |
| Konular: | |
| Online Erişim: | https://doi.org/10.1186/s12886-023-02905-5 |
| Etiketler: |
Etiket eklenmemiş, İlk siz ekleyin!
|