FSCN2 Gene Details
Disease Name: Retinitis pigmentosa
Chromosomal Location: Chromosome 17, NC_000017.11 (81515062..81537130)
Nucleotide Accession:
Mode of Inheritence: Autosomal dominant inheritance
Disease Name: Retinitis pigmentosa
Chromosomal Location: Chromosome 17, NC_000017.11 (81515062..81537130)
Nucleotide Accession:
Mode of Inheritence: Autosomal dominant inheritance