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PubMed

Záznam pochází z PubMed

COX6A1 mutation causes axonal hereditary motor and sensory neuropathy - the confirmation of the primary report

Laššuthová, P
Autor Laššuthová, P Department of Paediatric Neurology, DNA Laboratory, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
Beharka, R
Autor Beharka, R Department of Medical Genetics, The University Hospital Brno, Brno, Czech Republic
Krůtová, M
Autor Krůtová, M Department of Paediatric Neurology, DNA Laboratory, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
Neupauerová, J
Autor Neupauerová, J Department of Paediatric Neurology, DNA Laboratory, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
Seeman, P
Autor Seeman, P Department of Paediatric Neurology, DNA Laboratory, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic

Clinical genetics. 2016 Apr ; 89 (4) : 512-514. [epub] 20150825

Clin Genet
ISSN 1399-0004 | 0009-9163
Zdroj

Status PubMed-not-MEDLINE Jazyk angličtina Země Dánsko Médium print-electronic

Typ dokumentu dopisy

Perzistentní odkaz https://www.medvik.cz/link/pmid26302975

PubMed 26302975
DOI 10.1111/cge.12649
Knihovny.cz E-zdroje

Publikační typ
dopisy MeSH

Department of Medical Genetics The University Hospital Brno Brno Czech Republic

Department of Paediatric Neurology DNA Laboratory 2nd Faculty of Medicine Charles University Prague and University Hospital Motol Prague Czech Republic

Citace poskytuje Crossref.org

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Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients

Scientific reports. 2021 Apr 19 ; 11 (1) : 8443. [epub] 20210419

Sci Rep
ISSN 2045-2322
Zdroj

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