Publication | Closed Access

Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia

Thumb HypoplasiaDevelopmental BiologyMendelian DisorderGenetic DisorderSnx10 GeneGeneticsPathologyConsanguineous Iraqi BoyMolecular GeneticsMedical GeneticsMedicineHomozygous Stop Mutation