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A novel Gln358Glu mutation in ectodysplasin A associated with X‐linked dominant incisor hypodontia
Author(s) -
Tarpey Patrick,
Pemberton Trevor J.,
Stockton David W.,
Das Parimal,
Ninis Vasiliki,
Edkins Sarah,
Andrew Futreal P.,
Wooster Richard,
Kamath Sushanth,
Nayak Rabindra,
Stratton Michael R.,
Patel Pragna I.
Publication year - 2007
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.31567
Subject(s) - library science , medicine , computer science
Patrick Tarpey, Trevor J. Pemberton, David W. Stockton, Parimal Das, Vasiliki Ninis, Sarah Edkins, P. Andrew Futreal, Richard Wooster, Sushanth Kamath, Rabindra Nayak, Michael R. Stratton, and Pragna I. Patel* Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK Institute for Genetic Medicine, University of Southern California, Los Angeles, California Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, California Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas Department of Internal Medicine, Baylor College of Medicine, Houston, Texas Department of Ophthalmology, Baylor College of Medicine, Houston, Texas Department of Neurology, Baylor College of Medicine, Houston, Texas Kasturba Medical College, Mangalore, India Ambedkar Medical College, Kadugondanahalli, Bangalore, India Departments of Pediatrics and Internal Medicine, Wayne State University School of Medicine, Detroit, Michigan