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

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 f...

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Bibliographic Details
Main Authors: Heike Kölbel, Berthold P Hauffa, Stefan A Wudy, Anastasios Bouikidis, Adela Della Marina, Ulrike Schara
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5344335?pdf=render

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http://europepmc.org/articles/PMC5344335?pdf=render

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