Publication | Closed Access
Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort
101
Citations
20
References
2012
Year
Mendelian DisorderGenetic DisorderUk CohortGeneticsMedicineGenetic EpidemiologyAutonomic NeuropathyGenetic FactorNeurologyNeuroscienceDisease Gene IdentificationPublic HealthNeuropathologyMonogenic DisordersHereditary SensoryClinical Genetics
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