Clinical Features of Childhood Primary Ciliary Dyskinesia by Genotype and Ultrastructural Phenotype

Carson, Johnny L.; Cooper, Matthew L.; Davis, Stephanie D.; Dell, Sharon D.; Ferkol, Thomas W.; Hazucha, Milan J.; Knowles, Michael R.; Krischer, Jeffrey P.; Lee, Hye-Seung; Leigh, Margaret W.; Milla, Carlos; Pittman, Jessica E.; Rosenfeld, Margaret; Sagel, Scott D.; Shapiro, Adam J.; Zariwala, Maimoona A.

Clinical Features of Childhood Primary Ciliary Dyskinesia by Genotype and Ultrastructural Phenotype

Authors: Johnny L. Carson
Matthew L. Cooper
Stephanie D. Davis
Sharon D. Dell
Thomas W. Ferkol
Milan J. Hazucha
Michael R. Knowles
Jeffrey P. Krischer
Hye-Seung Lee
Margaret W. Leigh
Carlos Milla
Jessica E. Pittman
Margaret Rosenfeld
Scott D. Sagel
Adam J. Shapiro
Maimoona A. Zariwala
Publication date: 1 January 2015
Publisher
Doi

Abstract

Rationale: The relationship between clinical phenotype of childhood primary ciliary dyskinesia (PCD) and ultrastructural defects and genotype is poorly defined

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