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.