Publication | Closed Access
Familial schwannomatosis with a germline mutation of SMARCB1 in Japan
16
Citations
12
References
2015
Year
Neuro-oncologyRare DiseasesMendelian DisorderGenetic DisorderGeneticsPathologyNeurogeneticsDisease Gene IdentificationGermline MutationNeuropathologyMedicineClinical Genetics
| Year | Citations | |
|---|---|---|
Page 1
Page 1