HCRT Gene Details
Disease Name: Parkinson’s disease
Chromosomal Location: Chromosome 17, NC_000017.11 (42184060..42185452)
Nucleotide Accession: NG_011448.1
Mode of Inheritence: Autosomal dominant inheritance
Disease Name: Parkinson’s disease
Chromosomal Location: Chromosome 17, NC_000017.11 (42184060..42185452)
Nucleotide Accession: NG_011448.1
Mode of Inheritence: Autosomal dominant inheritance