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The ABCC6 Transporter as a Paradigm for Networking from an Orphan Disease to Complex Disorders
The knowledge on the genetic etiology of complex disorders largely results from the study of rare monogenic disorders. Often these common and rare diseases show phenotypic overlap, though monogenic diseases generally have a more extreme symptomatology. ABCC6, the gene responsible for pseudoxanthoma...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi Publishing Corporation
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555454/ https://www.ncbi.nlm.nih.gov/pubmed/26356190 http://dx.doi.org/10.1155/2015/648569 |