PRRT2 Gene Details
Disease Name: Hereditary spastic paraplegia
Chromosomal Location: Chromosome 16, NC_000016.10
Nucleotide Accession: NM_001256442.2
Mode of Inheritence: Autosomal dominant inheritance
Disease Name: Hereditary spastic paraplegia
Chromosomal Location: Chromosome 16, NC_000016.10
Nucleotide Accession: NM_001256442.2
Mode of Inheritence: Autosomal dominant inheritance