Publication | Closed Access
Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients
38
Citations
24
References
2011
Year
Genetic DisorderMedicineGeneticsGenetic EpidemiologyHuman PolymorphismPathologyMolecular GeneticsTunisian PatientsDisease Gene IdentificationMolecular DiagnosticsBioinformaticsOccludin Genes
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