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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
D.A. Spandidos
2018
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| 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 |