Publication | Closed Access
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy
37
Citations
7
References
2005
Year
Allelic VariantMendelian DisorderGenetic DisorderMedicineGeneticsClinical GeneticsPathologyGne Gene MutationMolecular GeneticsDisease Gene IdentificationTunisian FamiliesAllelic HeterogeneityMonogenic Disorders
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