Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III

BACKGROUND: Autosomal-recessive proximal spinal muscular atrophies (SMA) are disorders characterized by a ubiquitous deficiency of the survival of motor neuron protein that leads to a multisystemic disorder, which mostly affects alpha motor neurons. Disease progression is clinically associated with...

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Detalles Bibliográficos
Autores principales: Kölbel, Heike, Hauffa, Berthold P., Wudy, Stefan A., Bouikidis, Anastasios, Della Marina, Adela, Schara, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344335/
https://www.ncbi.nlm.nih.gov/pubmed/28278160
http://dx.doi.org/10.1371/journal.pone.0173144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344335/
https://www.ncbi.nlm.nih.gov/pubmed/28278160
http://dx.doi.org/10.1371/journal.pone.0173144

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