Síndrome de Bardet Biedl: rara causa de enfermedad renal terminal
Bardet Biedl syndrome (SBB) is a rare genetic disorder; its prevalence in North America and Europe is estimated at 1: 140,000 to 1: 160,000 newborns. It is included in the group of ciliopathies as it results from at least 16 different gene mutations suspected of playing a fundamental role in the cil...
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| Other Authors: | , , , |
| Format: | article |
| Language: | spa |
| Published: |
2016
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| Online Access: | https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/2853 |
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