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Genotype-Phenotype Relationships and Endocrine Findings in Prader-Willi Syndrome
Prader-Willi syndrome (PWS) is a complex imprinting disorder related to genomic errors that inactivate paternally-inherited genes on chromosome 15q11-q13 with severe implications on endocrine, cognitive and neurologic systems, metabolism, and behavior. The absence of expression of one or more genes...
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| Publicado no: | Front Endocrinol (Lausanne) |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6923197/ https://ncbi.nlm.nih.gov/pubmed/31920975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2019.00864 |
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