miércoles, 20 de diciembre de 2017

New Articles From Orphanet Journal of Rare Diseases

New Articles For BioMed Central:

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases

RESEARCH

Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients

Sandro Manuel Mueller, Saskia Maria Gehrig, Jens A. Petersen, Sebastian Frese, Violeta Mihaylova, Maria Ligon-Auer, Natalia Khmara, Jean-Marc Nuoffer, André Schaller, Carsten Lundby, Marco Toigo and Hans H. Jung
Orphanet Journal of Rare Diseases 2017, 12:184 | Published on: 19 December 2017

LETTER TO THE EDITOR

Novel SEA and LG2 Agrin mutations causing congenital Myasthenic syndrome

Jianying Xi, Chong Yan, Wei-Wei Liu, Kai Qiao, Jie Lin, Xia Tian, Hui Wu, Jiahong Lu, Lee-Jun Wong, David Beeson and Chongbo Zhao
Orphanet Journal of Rare Diseases 2017, 12:182 | Published on: 19 December 2017

REVIEW

KBG syndrome

Dayna Morel Swols, Joseph Foster and Mustafa Tekin
Orphanet Journal of Rare Diseases 2017, 12:183 | Published on: 19 December 2017

RESEARCH

Down-regulation of miR-9* in the peripheral leukocytes of Huntington’s disease patients

Kuo-Hsuan Chang, Yih-Ru Wu and Chiung-Mei Chen
Orphanet Journal of Rare Diseases 2017, 12:185 | Published on: 19 December 2017

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