GM2 Gangliosidosis in Shiba Inu Dogs with an In-Frame Deletion in HEXB-Reference-Cited by-同舟云学术

GM2 Gangliosidosis in Shiba Inu Dogs with an In-Frame Deletion in HEXB

Published:2017-08-20 Issue:5 Volume:31 Page:1520-1526
ISSN:0891-6640
Container-title:Journal of Veterinary Internal Medicine
language:en
Short-container-title:J Vet Intern Med

Author:

Kolicheski A.¹,Johnson G.S.¹^ORCID,Villani N.A.¹,O'Brien D.P.²,Mhlanga-Mutangadura T.¹,Wenger D.A.³,Mikoloski K.⁴,Eagleson J.S.⁵,Taylor J.F.⁶,Schnabel R.D.⁷,Katz M.L.⁸

Affiliation:

1. Department of Veterinary Pathobiology; University of Missouri; Columbia MO

2. Department of Veterinary Medicine and Surgery; University of Missouri; Columbia MO

3. Department of Neurology; Jefferson Medical College; Philadelphia PA

4. Pittsburgh Veterinary Specialty and Emergency Center; Pittsburgh PA

5. Veterinary Specialty and Emergency Center; Blue Pearl Veterinary Partners; Levittown PA

6. Division of Animal Sciences; University of Missouri; Columbia MO

7. Division of Animal Sciences and Informatics Institute; University of Missouri; Columbia MO

8. Mason Eye Institute; University of Missouri; Columbia MO

Funder

American Kennel Club Canine Health Foundation

Publisher

Wiley

Subject

General Veterinary

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jvim.14794/fullpdf

Reference35 articles.

1. A CLN8 nonsense mutation in the whole genome sequence of a mixed breed dog with neuronal ceroid lipofuscinosis and Australian Shepherd ancestry;Guo;Mol Genet Metab,2014

2. GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: A potential model for Tay Sachs disease;Sanders;Mol Genet Metab,2013

3. A novel mutation in the gene for canine acid beta-galactosidase that causes GM1-gangliosidosis in Shiba dogs;Yamato;J Inherit Metab Dis,2002

4. A rare homozygous MFSD8 single-base-pair deletion and frameshift in the whole genome sequence of a Chinese Crested dog with neuronal ceroid lipofuscinosis;Guo;BMC Vet Res,2014

5. Golden Retriever dogs with neuronal ceroid lipofuscinosis have a two-base-pair deletion and frameshift in CLN5;Gilliam;Mol Genet Metab,2015

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