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Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A v..:
Bueno, André S.
;
Nunes, Kelly
;
Dias, Alex M. M.
...
European Journal of Human Genetics. 30 (2021) 1 - p. 13-21 , 2021
Link:
https://doi.org/10.1038/s41431-021-00891-0
RT Journal T1
Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_s41431-021-00891-0&Exemplar=1&LAN=DE A1 Bueno, André S. A1 Nunes, Kelly A1 Dias, Alex M. M. A1 Alves, Leandro U. A1 Mendes, Beatriz C. A. A1 Sampaio-Silva, Juliana A1 Smits, Jeroen A1 Yntema, Helger G. A1 Meyer, Diogo A1 Lezirovitz, Karina A1 Mingroni-Netto, Regina C. PB Springer Science and Business Media LLC YR 2021 SN 1018-4813 SN 1476-5438 JF European Journal of Human Genetics VO 30 IS 1 SP 13 OP 21 LK http://dx.doi.org/https://doi.org/10.1038/s41431-021-00891-0 DO https://doi.org/10.1038/s41431-021-00891-0 SF ELIB - SuUB Bremen
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