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MYO5A Frameshift Variant in a Miniature Dachshund with Coat Color Dilution and Neurological Defects Resembling Human Griscelli Syndrome Type 1.
Christen, Matthias; de le Roi, Madeleine; Jagannathan, Vidhya; Becker, Kathrin; Leeb, Tosso.
Affiliation
  • Christen M; Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.
  • de le Roi M; Department of Pathology, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
  • Jagannathan V; Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.
  • Becker K; Department of Pathology, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
  • Leeb T; Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland.
Genes (Basel) ; 12(10)2021 09 23.
Article in En | MEDLINE | ID: mdl-34680875
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pigmentation Disorders / Piebaldism / Myosin Heavy Chains / Genetic Predisposition to Disease / Myosin Type V / Dog Diseases / Hearing Loss, Sensorineural Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Genes (Basel) Year: 2021 Document type: Article Affiliation country: Switzerland Country of publication: Switzerland
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pigmentation Disorders / Piebaldism / Myosin Heavy Chains / Genetic Predisposition to Disease / Myosin Type V / Dog Diseases / Hearing Loss, Sensorineural Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Genes (Basel) Year: 2021 Document type: Article Affiliation country: Switzerland Country of publication: Switzerland