Cover Image

Trinucleotide diseases and instability /

Show other versions (2)

The discovery in 1991 that human diseases can be caused by large-scale expansion of highly unstable trinucleotide repeats has elucidated a new mutation mechanism: heritable unstable DNA. There are ten possible trinucleotide repeats at the DNA level, but only three have been identified to be involved...

Full description

Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Oostra, Ben A., 1946-
Format: eBook
Language:English
Published: Berlin ; New York : Springer, [1998]
Series:Results and problems in cell differentiation ; 21.
Subjects:
Nervous system > Diseases > Genetic aspects.
Neurogenetics.
Human chromosome abnormalities.
Trinucleotide Repeats > genetics.
Chromosome Aberrations.
Fragile X Syndrome > genetics.
Huntington Disease > genetics.
Myotonic Dystrophy > genetics.
Life Sciences.
Cell Biology.
Molecular Medicine.
Human Genetics.
Système nerveux > Maladies > Aspect génétique.
Neurogénétique.
Chromosomes humains > Anomalies.
Chromosomes humains > Malformations.
Génétique.
Système nerveux maladies > génétique.
Aberration chromosomique, maladies.
Syndrome du chromosome X fragile.
Maladie de Huntington.
Développement neurologique.
Huntington-Chorea.
Myotonische Dystrophie.
Repeats.
DNS-Sequenz.
Pathophysiologie.
Fragiles-X-Syndrom.
Molekulargenetik.
Electronic books.
Online Access:Connect to the full text of this electronic book

Internet

Connect to the full text of this electronic book

Available Online

Holdings details from Available Online
Call Number: QH607 .R4 vol.21eb
 
Call Number Status Get It
QH607 .R4 vol.21eb Available