Literature DB >> 1709135

Correction of the published sequence for the human proteolipid protein gene.

P J Wilkins1, C R D'Souza, P J Bridge.   

Abstract

In the human proteolipid protein gene, the base sequence of the intronic region 5' to exon 6 was found to be 5'-ctctttcattttcctgcag-3' and not 5'-ctctttt-cattttcctgcag-3' as previously reported.

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Year:  1991        PMID： 1709135     DOI： 10.1007/bf00201552

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  4 in total

1.  Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder.

Authors:  L D Hudson; C Puckett; J Berndt; J Chan; S Gencic
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

2.  Individual exons encode the integral membrane domains of human myelin proteolipid protein.

Authors:  H J Diehl; M Schaich; R M Budzinski; W Stoffel
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205

3.  Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein.

Authors:  S Gencic; D Abuelo; M Ambler; L D Hudson
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

4.  Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant.

Authors:  J A Trofatter; S R Dlouhy; W DeMyer; P M Conneally; M E Hodes
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205
  4 in total

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