Yüklüyor......

Identification of a Mutation in the Novel Compound Heterozygous CFTR in a Chinese Family with Cystic Fibrosis

Cystic fibrosis (CF) is one of the most common autosomal recessive disorders among Caucasians of Northern European descent but is uncommon in the Chinese population. Objectives. To elucidate the mutation in the novel compound heterozygous CFTR causing CF in Chinese family. Materials and Methods. Cli...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Can Respir J
Asıl Yazarlar: Shao, Hongxia, Hua, Jingna, Wu, Qi, Li, Xiaoge, Zhang, Ming, Wang, Herong, Wu, Junping, Xu, Long, Xie, Yi, Li, Li, Chen, Huaiyong
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Hindawi 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7229557/
https://ncbi.nlm.nih.gov/pubmed/32454915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/6507583
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!