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1 Ergebnisse
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Variant c.2158-2A>G in MANBA is an important and frequent c..:
Safka Brozkova, Dana
;
Varga, Lukas
;
Uhrova Meszarosova, Anna
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448337/. , 2020
Link:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448337/
RT Journal T1
Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant
UL https://suche.suub.uni-bremen.de/peid=base-ftpubmed:oai:pubmedcentral.nih.gov:7448337&Exemplar=1&LAN=DE A1 Safka Brozkova, Dana A1 Varga, Lukas A1 Uhrova Meszarosova, Anna A1 Slobodova, Zuzana A1 Skopkova, Martina A1 Soltysova, Andrea A1 Ficek, Andrej A1 Jencik, Jan A1 Lastuvkova, Jana A1 Gasperikova, Daniela A1 Seeman, Pavel PB BioMed Central YR 2020 K1 Research JF http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448337/ LK http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448337/ DO http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448337/ SF ELIB - SuUB Bremen
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