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1. An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X)


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2. An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X)

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1739705
http://www.ncbi.nlm.nih.gov/pubmed/15965226  
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3. The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder


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4. 1106 The clinical phenotypic spectrum of GFPT1 associated congenital myasthenic syndrome


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5. The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1735862
http://www.ncbi.nlm.nih.gov/pubmed/15286164  
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6. Molecular characterisation of congenital myasthenic syndromes in Southern Brazil


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7. Molecular characterisation of congenital myasthenic syndromes in Southern Brazil


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8. CCDC 267626: Experimental Crystal Structure Determination


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9. CCDC 267627: Experimental Crystal Structure Determination


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10. CCDC 148383: Experimental Crystal Structure Determination


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