Primäre Ziliäre Dyskinesie (PCD) - Bobtail option-set-443684-checkbox-1 Mutations altering the sequence can

Mutations altering the sequence can lead to disruptions of the collagen structure

secondary hyperparathyroidism

translucent

Allele at is responsible for black-and-tan or tricolor phenotype

CMR1 is found in different dog breeds

Primäre Ziliäre Dyskinesie (PCD) - Bobtail option-set-443684-checkbox-1 Mutations altering the sequence canPrimary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder characterized by abnormally functioning cilia. The main clinical signs are recurrent or persistent respiratory infections because of the lack of effective ciliary motility. Other clinical signs include left right body asymmetry due to disruption of embryonic development and impaired male fertility due to defects of the spermatozoa flagella. Primary ciliary dyskinesia (PCD) is an