Cystic fibrosis presentation in del. F508 and p. Tyr109Glyfs compound heterozygote CFTR state: a case report

The diagnosis of cystic fibrosis (CF) is commonly confirmed by molecular genetics with the presence of specific mutations of cystic fibrosis transmembrane conductance regulator (CFTR) gene. We report a case of cystic fibrosis (CF) in a 15-year-old female patient who is a compound heterozygote for CF...

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Detalles Bibliográficos
Autores principales: Turkalj, Mirjana, Matišić, Vid, Šimić, Arijana, Juginović, Alen, Erceg, Damir, Drinković, Dorian Tješić, Höppner, Wolfgang, Primorac, Dragan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Medical Schools 2019
Materias:
11th ISABS CONFERENCE
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563179/
https://www.ncbi.nlm.nih.gov/pubmed/31187952
http://dx.doi.org/10.3325//cmj.2019.60.246

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563179/
https://www.ncbi.nlm.nih.gov/pubmed/31187952
http://dx.doi.org/10.3325//cmj.2019.60.246

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