
Mutations of DNAI1 in Primary Ciliary Dyskinesia: Evidence of Founder Effect in a Common Mutation
Author(s) -
Maimoona A. Zariwala,
Margaret W. Leigh,
F. Ceppa,
Marcus P. Kennedy,
Peadar G. Noone,
Johnny L. Carson,
Milan J. Hazucha,
Adriana Lori,
Judit Horváth,
Heike Olbrich,
Niki T. Loges,
Anne-Marie Bridoux,
Gaëlle Pennarun,
Bénédicte Duriez,
Estelle Escudier,
Hannah M. Mitchison,
Rahul Chodhari,
Eddie M.K. Chung,
Lucy C. Morgan,
Robbert U. de Iongh,
J Rutland,
Ugo Pradal,
Heymut Omran,
Serge Amselem,
Michael R. Knowles
Publication year - 2006
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/evkw-v287
Subject(s) - primary ciliary dyskinesia , mutation , founder effect , genetics , dyskinesia , biology , primary (astronomy) , medicine , gene , genotype , disease , parkinson's disease , bronchiectasis , haplotype , lung , physics , astronomy