Učitavanje...

Characterization of a novel pathogenic variation c.1237T>G in the FZD4 gene presenting new inheritance from an Iranian individual suffering vitreoretinopathy

Whole Exome Sequencing (WES) has been used increasingly in genetic determination of various known and unknown genetic disorders. Various genes are involved in the development of the vascular network of retina. Assessment of a collection of these genes could be provided by WES. Here we used WES for a...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:Intractable Rare Dis Res
Glavni autori: Zamani, Mina, Shariati, Gholamreza, Seifi, Tahereh, Sedaghat, Alireza, Galehdari, Hamid
Format: Artigo
Jezik:Inglês
Izdano: International Research and Cooperation Association for Bio & Socio-Sciences Advancement 2020
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7062596/
https://ncbi.nlm.nih.gov/pubmed/32201676
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2019.01109
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!