A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch-German) Mennonite and Hutterite patients in North America
Am J Med Genet A
.
2012 May;158A(5):1229-32.
doi: 10.1002/ajmg.a.35302.
Epub 2012 Apr 11.
Authors
Catrina Loucks
1
,
Jillian S Parboosingh
,
Jessica X Chong
,
Carole Ober
,
Victoria M Siu
,
Robert A Hegele
,
C Anthony Rupar
,
D Ross McLeod
,
Alfredo Pinto
,
Albert E Chudley
,
A Micheil Innes
Affiliation
1
Department of Medical Genetics, Alberta Children's Hospital and Alberta Children's Hospital Research Institute for Child and Maternal Health, University of Calgary, Calgary, Alberta, Canada.
PMID:
22495976
PMCID:
PMC4247856
DOI:
10.1002/ajmg.a.35302
No abstract available
Publication types
Research Support, Non-U.S. Gov't
MeSH terms
Ethnicity / genetics
Female
Founder Effect*
Genotype
Humans
Infant, Newborn
Male
Mutation*
North America
Protestantism
White People / genetics
Grants and funding
R01 HD021244/HD/NICHD NIH HHS/United States
R01 HL085197/HL/NHLBI NIH HHS/United States
CAPMC/ CIHR/Canada