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Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I

Molecular NeuroscienceGenetic DisorderGeneticsClinical GeneticsSerine PalmitoyltransferaseMolecular BiologyChain Base Subunit-1Molecular GeneticsDisease Gene IdentificationMedicineGenetic BasisNeurogenetics