Literature DB >> 9668233

Congenital myasthenic syndromes. New insights from molecular genetic and patch-clamp studies.

A G Engel1, K Ohno, M Milone, S M Sine.   

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Year:  1998        PMID： 9668233     DOI： 10.1111/j.1749-6632.1998.tb10921.x

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


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  4 in total

Review 1.  Ion channel genes and human neurological disease: recent progress, prospects, and challenges.

Authors:  E C Cooper; L Y Jan
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

2.  Skeletal muscle IP3R1 receptors amplify physiological and pathological synaptic calcium signals.

Authors:  Haipeng Zhu; Bula J Bhattacharyya; Hong Lin; Christopher M Gomez
Journal:  J Neurosci       Date:  2011-10-26       Impact factor: 6.167

3.  Nicotinic receptor fourth transmembrane domain: hydrogen bonding by conserved threonine contributes to channel gating kinetics.

Authors:  C Bouzat; F Barrantes; S Sine
Journal:  J Gen Physiol       Date:  2000-05       Impact factor: 4.086

4.  COLQ-mutant Congenital Myasthenic Syndrome with Microcephaly: A Unique Case with Literature Review.

Authors:  Mohammad A Al-Muhaizea; Sulaiman Bazee Al-Mobarak
Journal:  Transl Neurosci       Date:  2017-07-20       Impact factor: 1.757
  4 in total

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