Literature DB >> 2909695

Congenital muscular dystrophy and epidermolysis bullosa simplex.

G Kletter1, O B Evans, J A Lee, B Melvin, A B Yates, H G Bock.   

Abstract

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Year:  1989        PMID： 2909695     DOI： 10.1016/s0022-3476(89)80614-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  4 in total

1.  Identification of the cytolinker protein plectin in neuronal cells - expression of a rodless isoform in neurons of the rat superior cervical ganglion.

Authors:  Ferdinand Steinboeck; Doris Kristufek
Journal:  Cell Mol Neurobiol       Date:  2005-11       Impact factor: 5.046

2.  Plectin regulates the organization of glial fibrillary acidic protein in Alexander disease.

Authors:  Rujin Tian; Martin Gregor; Gerhard Wiche; James E Goldman
Journal:  Am J Pathol       Date:  2006-03       Impact factor: 4.307

3.  Human milk and the preterm baby.

Authors:  A F Williams
Journal:  BMJ       Date:  1993-06-19

4.  A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy.

Authors:  S Chavanas; L Pulkkinen; Y Gache; F J Smith; W H McLean; J Uitto; J P Ortonne; G Meneguzzi
Journal:  J Clin Invest       Date:  1996-11-15       Impact factor: 14.808
  4 in total

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