Condition: ALPORT SYNDROME 3, AUTOSOMAL DOMINANT


rs573527081 in COL4A3;MFF-DT gene and ALPORT SYNDROME 3, AUTOSOMAL DOMINANT PMID 30828794 2019 Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.

rs1363680371 in MFF-DT;COL4A3 gene and ALPORT SYNDROME 3, AUTOSOMAL DOMINANT PMID 9195222 1997 The clinical spectrum of type IV collagen mutations.