Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations

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作者： Johnson, K. ^[1] ; Bertoli, M. ^[2] ; Phillips, L. ^[3] ; Toepf, A. ^[4] ; Claeys, K. ^[5] ; Stojanovic, V. Rakocevic ^[6] ; Peric, S. ^[7] ; Vissine, J. ^[8] ; Hahn, A. ^[9] ; Maddison, P. ; Akay, E. ; Bastian, A. ; Lusakowska, A. ; Lek, M. ; Xu, L. ; MacArthur, D. ; Straub, V.

作者单位： RWTH Aachen Univ Hosp, Aachen, Germany ^[1] Newcastle Univ, Newcastle Upon Tyne, Tyne & Wear, England ^[2] Univ Copenhagen, Copenhagen, Denmark ^[3] Massachusetts Gen Hosp, Boston, MA 02114 USA ^[4] Univ Belgrade, Belgrade, Serbia ^[5] Univ Giessen, Giessen, Germany ^[6] Queens Med Ctr, Nottingham, England ^[7] Med Univ Warsaw, Warsaw, Poland ^[8] Carol Davila Univ Med & Pharm, Bucharest, Romania ^[9]

发布时间 2020-08-12

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Neuromuscular disorders

2016年26卷Suppl.2期

S108-S109页

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Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations

Neuromuscular disorders

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Neuromuscular disorders

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Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations

Neuromuscular disorders

相似文献

Neuromuscular disorders

相关期刊

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