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High Plasma Neurotensin Levels in Children with Prader–Willi Syndrome

Prader-Willi syndrome (PWS) is an obesity-related genetic condition, most commonly due to a paternal deletion of the chromosome 15q11-q13 region. PWS is characterized by growth hormone deficiency, infantile hypotonia and feeding problems, hypogenitalism/hypogonadism, increased pain threshold and the...

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Detalles Bibliográficos
Publicado en:Am J Med Genet A
Main Authors: Butler, Merlin G., Nelson, Tommy A., Driscoll, Daniel J., Manzardo, Ann M.
Formato: Artigo
Idioma:Inglês
Publicado: 2015
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6686671/
https://ncbi.nlm.nih.gov/pubmed/25847417
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.37103
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