Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
Dohrn MF1,2, Glöckle N1, Mulahasanovic L1, Heller C1, Mohr J1, Bauer C1, Riesch E1, Becker A1, Battke F1, […]
Dohrn MF1,2, Glöckle N1, Mulahasanovic L1, Heller C1, Mohr J1, Bauer C1, Riesch E1, Becker A1, Battke F1, […]