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STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population.
Marková, Simona Poisson; Brozková, Dana Safka; Lassuthová, Petra; Mészárosová, Anna; Krutová, Marcela; Neupauerová, Jana; Rasková, Dagmar; Trková, Marie; Stanek, David; Seeman, Pavel.
Afiliación
  • Marková SP; 1 DNA Laboratory, Department of Paediatric Neurology, 2nd Faculty of Medicine, Motol University Hospital, Charles University in Prague , Prague, Czech Republic .
  • Brozková DS; 1 DNA Laboratory, Department of Paediatric Neurology, 2nd Faculty of Medicine, Motol University Hospital, Charles University in Prague , Prague, Czech Republic .
  • Lassuthová P; 1 DNA Laboratory, Department of Paediatric Neurology, 2nd Faculty of Medicine, Motol University Hospital, Charles University in Prague , Prague, Czech Republic .
  • Mészárosová A; 1 DNA Laboratory, Department of Paediatric Neurology, 2nd Faculty of Medicine, Motol University Hospital, Charles University in Prague , Prague, Czech Republic .
  • Krutová M; 1 DNA Laboratory, Department of Paediatric Neurology, 2nd Faculty of Medicine, Motol University Hospital, Charles University in Prague , Prague, Czech Republic .
  • Neupauerová J; 1 DNA Laboratory, Department of Paediatric Neurology, 2nd Faculty of Medicine, Motol University Hospital, Charles University in Prague , Prague, Czech Republic .
  • Rasková D; 2 Gennet , Prague, Czech Republic .
  • Trková M; 2 Gennet , Prague, Czech Republic .
  • Stanek D; 1 DNA Laboratory, Department of Paediatric Neurology, 2nd Faculty of Medicine, Motol University Hospital, Charles University in Prague , Prague, Czech Republic .
  • Seeman P; 1 DNA Laboratory, Department of Paediatric Neurology, 2nd Faculty of Medicine, Motol University Hospital, Charles University in Prague , Prague, Czech Republic .
Genet Test Mol Biomarkers ; 22(2): 127-134, 2018 Feb.
Article en En | MEDLINE | ID: mdl-29425068
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pérdida Auditiva / Proteínas de la Membrana / Mutación Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Genet Test Mol Biomarkers Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2018 Tipo del documento: Article País de afiliación: República Checa Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pérdida Auditiva / Proteínas de la Membrana / Mutación Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Genet Test Mol Biomarkers Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2018 Tipo del documento: Article País de afiliación: República Checa Pais de publicación: Estados Unidos