New Articles From Orphanet Journal of Rare Diseases

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 Full Text | PDF 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 Full Text | PDF REVIEW KBG syndrome Dayna Morel Swols, Joseph Foster and Mustafa Tekin Orphanet Journal of Rare Diseases 2017, 12:183 | Published on: 19 December 2017 Full Text | PDF 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 Full Text | PDF

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