A family with hypothyroidism caused by fatty acid synthase and apolipoprotein B receptor mutations

Hypothyroidism is a disease with a genetic component. The present study aimed to identify the potential causative gene mutation in a family with hypothyroidism and to investigate its potential pathology. DNA was extracted from the affected individual and his parents, maternal aunt and maternal grand...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Jianhua, Sun, Lizhi, Chen, Weijie, Yin, Xiao, Lu, Yong, Jiang, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236273/
https://www.ncbi.nlm.nih.gov/pubmed/30272292
http://dx.doi.org/10.3892/mmr.2018.9499