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Variable clinical severity in TANGO2 deficiency: Case series and literature review.
Schymick, Jennifer; Leahy, Peter; Cowan, Tina; Ruzhnikov, Maura R Z; Gates, Ryan; Fernandez, Liliana; Pramanik, Gopal; Yarlagadda, Vamsi; Wheeler, Matthew; Bernstein, Jonathan A; Enns, Gregory M; Lee, Chung.
Afiliação
  • Schymick J; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA.
  • Leahy P; Department of Pediatrics, Santa Clara Valley Health and Hospital System, San Jose, California, USA.
  • Cowan T; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA.
  • Ruzhnikov MRZ; Cook Children's Medical Center, Fort Worth, Texas, USA.
  • Gates R; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA.
  • Fernandez L; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.
  • Pramanik G; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA.
  • Yarlagadda V; Stanford Center for Undiagnosed Diseases, Stanford, California, USA.
  • Wheeler M; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA.
  • Bernstein JA; Stanford Center for Undiagnosed Diseases, Stanford, California, USA.
  • Enns GM; Stanford Center for Undiagnosed Diseases, Stanford, California, USA.
Am J Med Genet A ; 188(2): 473-487, 2022 02.
Article em En | MEDLINE | ID: mdl-34668327
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Rabdomiólise / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Adicionar na Minha BVS
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XML
PubMed Links
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Rabdomiólise / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos