Publication | Closed Access
Charcot-Marie-Tooth disease type 2CC due to a frameshift mutation of the neurofilament heavy polypeptide gene in an Austrian family
13
Citations
9
References
2019
Year
Genetic DisorderGeneticsPathologyMolecular GeneticsAustrian FamilyDisease Gene IdentificationNeuropathologyMedicineFrameshift MutationNeurogenetics
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