It appears no script is enabled within your browser. Please enable JavaScript to use this site.
Skip header and navigation
Home
View Selections:
0
Items
Help
Print
Old meets new: identifying founder mutations in genetic disease.
https://arctichealth.org/en/permalink/ahliterature263534
Source
CMAJ. 2015 Feb 3;187(2):93-4
Publication Type
Article
Date
Feb-3-2015
More detail
Author
Jane A Evans
Source
CMAJ. 2015 Feb 3;187(2):93-4
Date
Feb-3-2015
Language
English
Publication Type
Article
Keywords
Carbohydrate Metabolism, Inborn Errors - ethnology - genetics
Female
Founder Effect
Glycogen Debranching Enzyme System - genetics
Glycogen Storage Disease Type III - ethnology - genetics
Humans
Inuits - genetics
Male
Mutation - genetics
Sucrase-Isomaltase Complex - deficiency - genetics
Notes
Cites: Ann Neurol. 2002 Oct;52(4):506-1012325082
Cites: Am J Hum Genet. 1997 May;60(5):1079-849150155
Cites: Eur J Hum Genet. 1997 Sep-Oct;5(5):266-709412782
Cites: CMAJ. 2005 Feb 1;172(3):355-815684118
Cites: Am Fam Physician. 2005 Aug 1;72(3):386-716100853
Cites: Am Fam Physician. 2005 Aug 1;72(3):441-816100858
Cites: Fam Cancer. 2007;6(1):1-1217039271
Cites: Am J Hum Genet. 2014 Jun 5;94(6):809-1724906018
Cites: CMAJ. 2015 Feb 3;187(2):102-725452324
Cites: CMAJ. 2015 Feb 3;187(2):E68-7325602008
Cites: Mol Genet Metab. 2001 May;73(1):55-6311350183
Cites: Proc Natl Acad Sci U S A. 2002 Apr 2;99(7):4614-911904371
Comment On: CMAJ. 2015 Feb 3;187(2):102-725452324
Comment On: CMAJ. 2015 Feb 3;187(2):E68-7325602008
PubMed ID
25602001
View in PubMed
Less detail
Permalink