Open AccessLethal Skeletal Dysplasia in Mice and Humans Lacking the Golgin GMAP-210
Author(s) -
Patrick Smits,
Andrew D. Bolton,
Vincent Funari,
Minh Hong,
Eric D. Boyden,
Lei Lü,
Danielle K. Manning,
Noelle D. Dwyer,
Jennifer L. Moran,
Mary Prysak,
Barry Merriman,
Stanley F. Nelson,
Luisa Bonafé,
Andrea SupertiFurga,
Shiro Ikegawa,
Deborah Krakow,
Daniel H. Cohn,
Tomas Kirchhausen,
Matthew L. Warman,
David R. Beier
Publication year - 2010
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa0900158
Subject(s) - biology , microbiology and biotechnology , phenotype , genetics , mutation , gene
Establishing the genetic basis of phenotypes such as skeletal dysplasia in model organisms can provide insights into biologic processes and their role in human disease.
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