Concepedia

Publication | Open Access

Mutations of <i>DNAH11</i> in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

DOIFull Paper Access

223

Citations

40

References

2011

Year

Michael R. Knowles, Margaret W. Leigh, Johnny L. Carson, Stephanie D. Davis, Sharon Dell, Thomas W. Ferkol, Kenneth N. Olivier, Scott D. Sagel, Margaret Rosenfeld, Kimberlie A. Burns,
Thorax

Abstract

Mutations in DNAH11 are a common cause of PCD in patients without ciliary ultrastructural defects; thus, genetic analysis can be used to ascertain the diagnosis of PCD in this challenging group of patients.

References

YearCitations

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