Publication | Closed Access
A Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1C
21
Citations
28
References
2019
Year
Novel VariantGenetic DisorderGeneticsPathologyDegenerative DiseaseMolecular GeneticsMedical GeneticsDisease Gene IdentificationPeripheral NervesMedicineNeuropathologyNeurogenetics
| Year | Citations | |
|---|---|---|
Page 1
Page 1