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Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings
INTRODUCTION: Prader-Willi syndrome (PWS) is a multisystemic complex genetic disorder caused by lack of expression of genes on the paternally inherited chromosome 15q11.2-q13 region. There are three main genetic subtypes in PWS: paternal 15q11-q13 deletion (65–75 % of cases), maternal uniparental di...
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| Gepubliceerd in: | J Endocrinol Invest |
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| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Springer International Publishing
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4630255/ https://ncbi.nlm.nih.gov/pubmed/26062517 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40618-015-0312-9 |
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