Literature DB >> 10848501

Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3.

M M Lesperance, M Burmeister.   

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Year:  2000        PMID： 10848501      PMCID： PMC1287092          DOI： 10.1086/302975

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  2 in total

Review 1.  Genetic dissection of complex traits.

Authors:  E S Lander; N J Schork
Journal:  Science       Date:  1994-09-30       Impact factor: 47.728

2.  Localization of the gene for a novel autosomal recessive neurodegenerative Huntington-like disorder to 4p15.3.

Authors:  M Kambouris; S Bohlega; A Al-Tahan; B F Meyer
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025
  2 in total
  1 in total

1.  Huntington disease phenocopy is a familial prion disease.

Authors:  R C Moore; F Xiang; J Monaghan; D Han; Z Zhang; L Edström; M Anvret; S B Prusiner
Journal:  Am J Hum Genet       Date:  2001-10-09       Impact factor: 11.025
  1 in total

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