Open AccessMutations of DNAI1 in primary ciliary dyskinesia: Evidence of founder effect in a common mutation
Author(s) -
G. Pennarun,
L.C. Morgan,
E.M.K. Chung,
B. Duriez,
H. Olbrich,
S. Amselem,
J. Rutland,
H.M. Mitchison,
M.A. Zariwala,
N.T. Loges,
J.L. Carson,
M.W. Leigh,
R.U. De Iongh,
R. Chodhari,
P.G. Noone,
H. Omran,
M.P. Kennedy,
U. Pradal,
M.R. Knowles,
A. Lori,
E. Escudier,
A.-M. Bridoux,
F. Ceppa,
J. Horvath,
M.J. Hazucha
Publication year - 2020
Publication title -
unc libraries
Language(s) - English
DOI - 10.17615/v9jr-g496
Subject(s) - primary ciliary dyskinesia , genetics , mutation , founder effect , dyskinesia , biology , medicine , gene , genotype , bronchiectasis , parkinson's disease , haplotype , lung , disease
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