Publication | Closed Access
Two novel CLN5 mutations in a Portuguese patient with vLINCL: Insights into molecular mechanisms of CLN5 deficiency
38
Citations
28
References
2006
Year
Cln5 DeficiencyMendelian DisorderGenetic DisorderGeneticsPathogenesisPathologyNovel Cln5 MutationsPortuguese PatientMolecular GeneticsDisease Gene IdentificationMedicineVariant Interpretation
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|---|---|---|
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