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Identification of the porcine homologous of human disease causing trinucleotide repeat sequences

✍ Scribed by Lone Bruhn Madsen; Bo Thomsen; Christina Ane Elisabeth Sølvsten; Christian Bendixen; Merete Fredholm; Arne Lund Jørgensen; Anders Lade Nielsen


Publisher
Springer
Year
2007
Tongue
English
Weight
349 KB
Volume
8
Category
Article
ISSN
1364-6745

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A relatively rare type of mutation causing human genetic disease is the indel, a complex lesion that appears to represent a combination of micro-deletion and micro-insertion. In the absence of meta-analytical studies of indels, the mutational mechanisms underlying indel formation remain unclear. Dat