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1 Ergebnisse
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Rare mutations in ATL3, SPTLC2 and SCN9A explaining heredit..:
Cintra, Vivian Pedigone
;
Dohrn, Maike F.
;
Tomaselli, Pedro José
...
Journal of the Neurological Sciences. 427 (2021) - p. 117498 , 2021
Link:
https://doi.org/10.1016/j.jns.2021.117498
RT Journal T1
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohort
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.jns.2021.117498&Exemplar=1&LAN=DE A1 Cintra, Vivian Pedigone A1 Dohrn, Maike F. A1 Tomaselli, Pedro José A1 Figueiredo, Fernanda Barbosa A1 Marques, Sandra Elisabete A1 Camargos, Sarah Teixeira A1 Barbosa, Luiz Sergio Mageste A1 P. Rebelo, Adriana A1 Abreu, Lisa A1 Danzi, Matt A1 Marques Jr, Wilson A1 Züchner, Stephan PB Elsevier BV YR 2021 SN 0022-510X JF Journal of the Neurological Sciences VO 427 SP 117498 LK http://dx.doi.org/https://doi.org/10.1016/j.jns.2021.117498 DO https://doi.org/10.1016/j.jns.2021.117498 SF ELIB - SuUB Bremen
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