Lung disease associated with filamin A gene mutation: a case report

BACKGROUND: Mutations in the gene encoding filamin A (FLNA) lead to diseases with high phenotypic diversity including periventricular nodular heterotopia, skeletal dysplasia, otopalatodigital spectrum disorders, cardiovascular abnormalities, and coagulopathy. FLNA mutations were recently found to be...

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Detalles Bibliográficos
Autores principales: Eltahir, Safa, Ahmad, Khalid S., Al-Balawi, Mohammed M., Bukhamsien, Hussien, Al-Mobaireek, Khalid, Alotaibi, Wadha, Al-Shamrani, Abdullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836084/
https://www.ncbi.nlm.nih.gov/pubmed/27091362
http://dx.doi.org/10.1186/s13256-016-0871-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836084/
https://www.ncbi.nlm.nih.gov/pubmed/27091362
http://dx.doi.org/10.1186/s13256-016-0871-1

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