Literature DB >> 9668236

Congenital myasthenic syndromes. Studies of the AChR and other candidate genes.

D Beeson1, C Newland, R Croxen, A Buckel, F Y Li, C Larsson, M Tariq, A Vincent, J Newsom-Davis.   

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Year:  1998        PMID： 9668236     DOI： 10.1111/j.1749-6632.1998.tb10924.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN： 0077-8923            Impact factor:   5.691


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  2 in total

1.  Selective cleavage of AChR cRNAs harbouring mutations underlying the slow channel myasthenic syndrome by hammerhead ribozymes.

Authors:  Amr Abdelgany; John Ealing; Matthew Wood; David Beeson
Journal:  J RNAi Gene Silencing       Date:  2005-07-28

2.  AChR deficiency due to epsilon-subunit mutations: two common mutations in the Netherlands.

Authors:  Catharina G Faber; Peter C Molenaar; Johannes S H Vles; Domenic M Bonifati; Jan J G M Verschuuren; Pieter A van Doorn; Jan B M Kuks; John H J Wokke; David Beeson; Marc De Baets
Journal:  J Neurol       Date:  2009-06-21       Impact factor: 4.849
  2 in total

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