| Literature DB >> 9932964 |
M A Nance1, V Mathias-Hagen, G Breningstall, M J Wick, R C McGlennen.
Abstract
A patient with juvenile Huntington's disease (HD) of probable maternal inheritance is reported. The expanded IT-15 allele was only detected with the use of modified PCR and Southern transfer techniques, which showed a CAG trinucleotide repeat expansion of approximately 250 repeats-the largest CAG expansion reported within the huntingtin gene. This case emphasizes the need for communication between the diagnostic laboratory and the clinician to define the molecular genetics of unusual cases.Entities:
Mesh:
Year: 1999 PMID: 9932964 DOI: 10.1212/wnl.52.2.392
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910