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Loss-of-function variants in POT1 predispose to uveal melanoma.
Nathan, Vaishnavi; Palmer, Jane M; Johansson, Peter A; Hamilton, Hayley R; Warrier, Sunil K; Glasson, William; McGrath, Lindsay A; Kahl, Vivian F S; Vasireddy, Raja S; Pickett, Hilda A; Brooks, Kelly M; Pritchard, Antonia L; Hayward, Nicholas K.
Afiliación
  • Nathan V; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Palmer JM; Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia.
  • Johansson PA; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Hamilton HR; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Warrier SK; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Glasson W; Queensland Ocular Oncology Services, The Terrace Eye Centre, Brisbane, Queensland, Australia.
  • McGrath LA; Queensland Ocular Oncology Services, The Terrace Eye Centre, Brisbane, Queensland, Australia.
  • Kahl VFS; Queensland Ocular Oncology Services, The Terrace Eye Centre, Brisbane, Queensland, Australia.
  • Vasireddy RS; Children's Medical Research Institute, University of Sydney, Westmead, New South Wales, Australia.
  • Pickett HA; Children's Hospital at Westmead, Sydney Children's Hospitals Network, Westmead, New South Wales, Australia.
  • Brooks KM; Children's Medical Research Institute, University of Sydney, Westmead, New South Wales, Australia.
  • Pritchard AL; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Hayward NK; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
J Med Genet ; 58(4): 234-236, 2021 04.
Article en En | MEDLINE | ID: mdl-32907878
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Úvea / Predisposición Genética a la Enfermedad / Proteínas de Unión a Telómeros / Melanoma Límite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Med Genet Año: 2021 Tipo del documento: Article País de afiliación: Australia
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Úvea / Predisposición Genética a la Enfermedad / Proteínas de Unión a Telómeros / Melanoma Límite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Med Genet Año: 2021 Tipo del documento: Article País de afiliación: Australia