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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...

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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:	Articles
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

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