PRPF31 Gene Details
Disease Name: Retinitis pigmentosa
Chromosomal Location: Chromosome 19, NC_000019.10 (54115754..54131713)
Nucleotide Accession:
Mode of Inheritence: Autosomal dominant inheritance
Disease Name: Retinitis pigmentosa
Chromosomal Location: Chromosome 19, NC_000019.10 (54115754..54131713)
Nucleotide Accession:
Mode of Inheritence: Autosomal dominant inheritance