Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD)

BACKGROUND: Mutations in the DNAI1 gene, encoding a component of outer dynein arms of the ciliary apparatus, are the second most important genetic cause of primary ciliary dyskinesia (PCD), the genetically heterogeneous recessive disorder with the prevalence of ~1/20,000. The estimates of the DNAI1...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Ziętkiewicz, Ewa, Nitka, Barbara, Voelkel, Katarzyna, Skrzypczak, Urszula, Bukowy, Zuzanna, Rutkiewicz, Ewa, Humińska, Kinga, Przystałowska, Hanna, Pogorzelski, Andrzej, Witt, Michał
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2010
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3014902/
https://ncbi.nlm.nih.gov/pubmed/21143860
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1465-9921-11-174
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados