File:Missense-Mutation-in-CAPN1-Is-Associated-with-Spinocerebellar-Ataxia-in-the-Parson-Russell-Terrier-pone.0064627.s008.ogv
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[edit]DescriptionMissense-Mutation-in-CAPN1-Is-Associated-with-Spinocerebellar-Ataxia-in-the-Parson-Russell-Terrier-pone.0064627.s008.ogv |
English: Parson Russell Terrier with SCA. 6 year, 4 month old, male neutered PRT with SCA. Note the characteristic prancing or dancing type of gait, especially affecting the pelvic limbs. There is truncal ataxia, impaired balance and pelvic limb hypermetria and spasticity. The owner of this PRT detected initial signs of SCA when the dog was approximately 10 months old. Progressive deterioration with periods of stabilisation has occurred. Neurological examination and BAEPs were consistent with those previously reported in PRTs and JRTs with hereditary ataxia. |
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Source | Video S1 from Forman O, De Risio L, Mellersh C (2013). "Missense Mutation in CAPN1 Is Associated with Spinocerebellar Ataxia in the Parson Russell Terrier Dog Breed". PLOS ONE. DOI:10.1371/journal.pone.0064627. PMID 23741357. PMC: 3669408. | ||
Author | Forman O, De Risio L, Mellersh C | ||
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 06:04, 13 June 2013 | 30 s, 960 × 540 (16.2 MB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Author | Forman O, De Risio L, Mellersh C |
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Usage terms | http://creativecommons.org/licenses/by/3.0/ |
Image title | Parson Russell Terrier with SCA. 6 year, 4 month old, male neutered PRT with SCA. Note the characteristic prancing or dancing type of gait, especially affecting the pelvic limbs. There is truncal ataxia, impaired balance and pelvic limb hypermetria and spasticity. The owner of this PRT detected initial signs of SCA when the dog was approximately 10 months old. Progressive deterioration with periods of stabilisation has occurred. Neurological examination and BAEPs were consistent with those previously reported in PRTs and JRTs with hereditary ataxia. |
Software used | |
Date and time of digitizing | 2013 |
Language | English |