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Whole genome sequencing identifies a homozygous nonsense mutation in the JPH2 gene in Shih Tzu dogs with progressive retinal atrophy.
Urkasemsin, G; Pongpanich, M; Sariya, L; Kongcharoen, A; Buddhirongawatr, R; Rungarunlert, S; Ferreira, J N; Chetruengchai, W; Phokaew, C; Srichomthong, C; Shotelersuk, V.
Afiliação
  • Urkasemsin G; Department of Preclinic and Applied Animal Science, Faculty of Veterinary Science, Mahidol University, Nakhon Pathom, 73170, Thailand.
  • Pongpanich M; Department of Mathematics and Computer Science, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand.
  • Sariya L; Age-related Inflammation and Degeneration Research Unit, Chulalongkorn University, Bangkok, 10330, Thailand.
  • Kongcharoen A; The Monitoring and Surveillance Center for Zoonotic Diseases in Wildlife and Exotic Animals, Faculty of Veterinary Science, Mahidol University, Nakhon Pathom, 73170, Thailand.
  • Buddhirongawatr R; Prasu-Arthorn Animal Hospital, Faculty of Veterinary Science, Mahidol University, Nakhon Pathom, 73170, Thailand.
  • Rungarunlert S; Department of Clinical Sciences and Public Health, Faculty of Veterinary Science, Mahidol University, Nakhon Pathom, 73170, Thailand.
  • Ferreira JN; Department of Preclinic and Applied Animal Science, Faculty of Veterinary Science, Mahidol University, Nakhon Pathom, 73170, Thailand.
  • Chetruengchai W; Exocrine Gland Biology and Regeneration Research Group, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, Thailand.
  • Phokaew C; Department of Pediatrics, Faculty of Medicine, Center of Excellence for Medical Genomics, Medical Genomics Cluster, Chulalongkorn University, Bangkok, 10330, Thailand.
  • Srichomthong C; Excellence Center for Genomics and Precision Medicine, King Chulalongkorn Memorial Hospital, The Thai Red Cross Society, Bangkok, 10330, Thailand.
  • Shotelersuk V; Department of Pediatrics, Faculty of Medicine, Center of Excellence for Medical Genomics, Medical Genomics Cluster, Chulalongkorn University, Bangkok, 10330, Thailand.
Anim Genet ; 52(5): 714-719, 2021 Oct.
Article em En | MEDLINE | ID: mdl-34231238
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Degeneração Retiniana / Códon sem Sentido / Doenças do Cão / Cães / Proteínas de Membrana / Proteínas Musculares Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Anim Genet Assunto da revista: GENETICA / MEDICINA VETERINARIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Tailândia
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Degeneração Retiniana / Códon sem Sentido / Doenças do Cão / Cães / Proteínas de Membrana / Proteínas Musculares Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Anim Genet Assunto da revista: GENETICA / MEDICINA VETERINARIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Tailândia