Analysis of the

The defect causing Huntington's disease (HD) has recently been discovered as an expanded CAG trinucleotide repeat located at the 5′ end of the IT15 gene. This discovery allows the molecular diagnosis of HD by measuring the CAG repeat length. The normal and pathological repeat ranges in a popula...

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Veröffentlicht in:	Human biology 1997-10, Vol.69 (5), p.653
Hauptverfasser:	Leone, O, Muglia, M, Gabriele, A.L, Annesi, G, Conforti, F.L, Imbrogno, E, Imbrogno, L, Brancati, C
Format:	Artikel
Sprache:	eng
Schlagworte:	Analysis Huntington's chorea Nucleotide sequence
Online-Zugang:	Volltext
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