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Growth Hormone Receptor (GHR) Gene Polymorphism and Prader-Willi Syndrome
Prader-Willi syndrome (PWS) is a genomic imprinting disorder due to loss of paternally expressed genes in the 15q11-q13 region and characterized by hypotonia, a poor suck, failure to thrive, hypogonadism/hypogenitalism, growth hormone deficiency, learning and behavioral problems and hyperphagia lead...
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| Autores principales: | , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2013
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3689873/ https://ncbi.nlm.nih.gov/pubmed/23696513 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.35980 |
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