SFX by Ex Libris Inc.

Title:	Huntington's gene: so near, yet so far
Source:	Science [0036-8075] Roberts, L yr:1990

Basic

Sorry, no full text available...

Please use the document delivery service (see below)

Holding information

Holdings in library search engine ALBERT

Document delivery

Request document via Library/Bibliothek

Users interested in this article also expressed an interest in the following:
description	1.	Morell, V. "Huntington's gene finally found. (includes related information on implications for genetic counseling)." Science 260.5104 (1993): 28-.
description	2.	Wheeler, V C, Persichetti, F, McNeil, S M, Mysore,, N S S. "Factors associated with HD CAG repeat instability in Huntington disease." Journal of medical genetics 44.11: 695-701.
description	3.	Semaka, A. "Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles)." American journal of medical genetics. Part B, Neuropsychiatric genetics 153B.1 (2009): 314-320.
description	4.	Ishiguro, H. "Age-dependent and tissue-specific CAG repeat instability occurs in mouse knock-in for a mutant Huntington's disease gene." Journal of neuroscience research 65.4 (2001): 289-97.
description	5.	Swami, M. "Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset." Human Molecular Genetics 18.16 (2009): 3039-3047.
description	6.	Walker, Francis O. "Huntington's disease." Lancet, The 369.9557 (2007): 218-228.
description	7.	Lander, Eric S. "Initial impact of the sequencing of the human genome.(Report)." Nature 470.7333 (2011): 187-.
description	8.	Quarrell, O. Juvenile Huntington's disease and other trinucleotide repeat disorders /. 2009.
description	9.	Barinaga M, M. "An intriguing new lead on Huntington's disease." Science 271.5253 (1996): 1233-1234.
description	10.	Wintrebert, Claire M A A. "Assessing genetic effects in survival data by correlating martingale residuals with an application to age at onset of Huntington disease." Statistics in medicine 25.18 (2006): 3190-3200.
description	11.	Andresen, J. "The Relationship Between CAG Repeat Length and Age of Onset Differs for Huntington's Disease Patients with Juvenile Onset or Adult Onset." Annals of human genetics 71.3 (2007): 295-301.
description	12.	Aubeeluck, A. "Huntington's disease. Part 1: essential background and management." British journal of nursing 17.3 (2008): 146-51.
description	13.	Kent, A. "Huntington's disease." Nursing standard 18.32 (2004): 45-51.
description	14.	Novak, Marianne J U J. "Huntington's disease." BMJ. British medical journal (Clinical research ed.) 340.30 (2010): 34-40.
description	15.	MARIAN, A. "Challenges in Medical Applications of Whole Exome/Genome Sequencing Discoveries." Trends in cardiovascular medicine 22.8 (2012): 219-223.
description	16.	Halpin, M. "Diagnosis, psychiatry and neurology: The case of Huntington Disease." Social science & medicine 73.6 (2011): 858-865.
description	17.	Ross, Christopher A. "Huntington's disease: from molecular pathogenesis to clinical treatment." Lancet neurology 10.1 (2011): 83-98.
description	18.	Rubinsztein, David C C. "Huntington's disease: molecular basis of neurodegeneration." Expert reviews in molecular medicine 5.20 (2003): 1-21.
description	19.	Aubeeluck, A. "Huntington's disease. Part 2: treatment and management issues in juvenile HD." British journal of nursing 17.4 (2008): 260-263.
description	20.	Kramerova, I. "Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle." Human Molecular Genetics 18.17 (2009): 3194-205.