Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness

Overview of attention for article published in Orphanet Journal of Rare Diseases, November 2017

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Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness https://t.co/PzEKz7KjKY

20 Nov 2017

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PubMed: Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness. https://t.co/thzTXJMtNy

19 Nov 2017

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RT @eerr_es: Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplain... https://t…

19 Nov 2017

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Wao! https://t.co/197LxjBEwX

19 Nov 2017

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