Publication | Closed Access
Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia
26
Citations
33
References
2013
Year
Hk1 GenesMendelian DisorderGenetic DisorderGeneticsNeuroepidemiologyClinical GeneticsInherited NeuropathiesNeurologyNeuropathologyMedicineFounder MutationsNeurogenetics
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