Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review
Adam J. Shapiro(McGill University Health Centre), Margaret W. Leigh(University of North Carolina at Chapel Hill)
Cited by 440
Related Papers
Mutations in <i>RSPH1</i> Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype
|American Journal of Respiratory and Critical Care Medicine|2014|229
ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6
|The American Journal of Human Genetics|2013|204
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
|The American Journal of Human Genetics|2013|201
Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms
|The American Journal of Human Genetics|2013|145