Next-generation panel sequencing identifies NF1 germline mutations in three patients with pheochromocytoma but no clinical diagnosis of neurofibromatosis type 1
- Laura Gieldon*
- , Jimmy Rusdian Masjkur
- , Susan Richter
- , Roland Därr
- , Marcos Lahera
- , Daniela Aust
- , Silke Zeugner
- , Andreas Rump
- , Karl Hackmann
- , Andreas Tzschach
- , Andrzej Januszewicz
- , Aleksander Prejbisz
- , Graeme Eisenhofer
- , Evelin Schrock
- , Mercedes Robledo
- , Barbara Klink
*Corresponding author for this work
Research output: Contribution to journal › Article › Research › peer-review
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Citations
(Scopus)