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@proceedings{882493, author = {Hermanová, Markéta and Stehlíková, Kristýna and Vondráček, Petr and Zámečník, Josef and Fajkusová, Lenka}, booktitle = {The 6th Symposium and Workshop on Molecular Pathology and Histo(cyto)chemistry.}, keywords = {limb-girdle muscular dystrophy; Czech Republic}, language = {eng}, isbn = {978-80-87327-07-4}, title = {Molecular diagnostics of limb-girdle muscular dystrophies.}, year = {2010} }
TY - CONF ID - 882493 AU - Hermanová, Markéta - Stehlíková, Kristýna - Vondráček, Petr - Zámečník, Josef - Fajkusová, Lenka PY - 2010 TI - Molecular diagnostics of limb-girdle muscular dystrophies. SN - 9788087327074 KW - limb-girdle muscular dystrophy KW - Czech Republic N2 - The diagnostic of limb-girdle muscular dystrophies needs to integrate clinical analysis, protein analysis in muscle biopsies, and genetic testing in specialized centres. In Czech Republic, the LGMD2A represent the most frequent LGMD, which was confirmed in 37 patients. In 6 patients the diagnosis of LGMD2I and LGMD2D was confirmed. ER -
HERMANOVÁ, Markéta, Kristýna STEHLÍKOVÁ, Petr VONDRÁČEK, Josef ZÁMEČNÍK a Lenka FAJKUSOVÁ. Molecular diagnostics of limb-girdle muscular dystrophies. In \textit{The 6th Symposium and Workshop on Molecular Pathology and Histo(cyto)chemistry.}. 2010. ISBN~978-80-87327-07-4.
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