Open AccessA universal mechanism ties genotype to phenotype in trinucleotide diseases
Author(s) -
Shai Kaplan,
Shalev Itzkovitz,
Ehud Shapiro
Publication year - 2005
Publication title -
plos computational biology
Language(s) - English
Resource type - Journals
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.0030235.eor
Subject(s) - trinucleotide repeat expansion , genetics , allele , biology , genotype , mechanism (biology) , ataxia , phenotype , disease , age of onset , huntington's disease , mutation , gene , medicine , neuroscience , pathology , philosophy , epistemology
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