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Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report.
Park, Joonhong; Yhim, Ho-Young; Kang, Kyung Pyo; Bae, Tae Won; Cho, Yong Gon.
Afiliação
  • Park J; Department of Laboratory Medicine, Jeonbuk National University Medical School and Hospital, Jeonju, Korea.
  • Yhim HY; Research Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital, Jeonju, Korea.
  • Kang KP; Department of Internal Medicine, Jeonbuk National University Medical School and Hospital, Jeonju, Korea.
  • Bae TW; Research Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital, Jeonju, Korea.
  • Cho YG; Department of Internal Medicine, Jeonbuk National University Medical School and Hospital, Jeonju, Korea.
Hematology ; 27(1): 603-608, 2022 Dec.
Article em En | MEDLINE | ID: mdl-35617302
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome Hemolítico-Urêmica Atípica Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome Hemolítico-Urêmica Atípica Idioma: En Ano de publicação: 2022 Tipo de documento: Article