Publication | Closed Access
Fh-Souassi: a founder frameshift mutation in exon 10 of the LDL-receptor gene, associated with a mild phenotype in Tunisian families
25
Citations
36
References
2001
Year
Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyHuman PolymorphismMolecular BiologyMolecular GeneticsExon 10Disease Gene IdentificationTunisian FamiliesMedicineMild PhenotypeClinical Genetics
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