MAPT Gene Details
Disease Name: Cerebral creatine deficiency syndrome
Chromosomal Location: Chromosome 17, NC_000017.11
Nucleotide Accession: AK095802.1 AK299658.1 AK299704.1 AY413628.1 BC000558.2 BC098281.1 BC099721.1 BC101936.1 BC114504.1 BC114948.1 BN000503.1 CH471233.1 CM000268.1 DN996935.1 DN997108.1 DR001556.1 DR001941.1 DR002467.1 FJ009034.1 FU774166.1 FU774167.1 FU774168.1
Mode of Inheritence: Autosomal dominant
