Publication | Open Access

Homozygous Missense Mutation in Fibulin-5 in an Iranian Autosomal Recessive Cutis Laxa Pedigree and Associated Haplotype

Developmental BiologyGenetic DisorderGeneticsHomozygous Missense MutationMolecular GeneticsGenetic VariationGenomicsApplied GeneticsMedicineAssociated Haplotype