GTP cyclohydrolase I gene in hereditary progressive dystonia with marked diurnal fluctuation.

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Citation

Ichinose H, Ohye T, Segawa M, Nomura Y, Endo K, Tanaka H, Tsuji S, Fujita K, Nagatsu T

GTP cyclohydrolase I gene in hereditary progressive dystonia with marked diurnal fluctuation.

Neurosci Lett. 1995 Aug 18;196(1-2):5-8.

PubMed ID
7501255 [ View in PubMed
]
Abstract

We previously reported four different mutations in the coding region of GTP cyclohydrolase I (GCH-I) gene in patients with hereditary progressive dystonia with marked diurnal fluctuation (HPD). We found two independent new mutations (leucine 79 proline and a deletion in exon 4) in patients with HPD. We also found four families of HPD without any mutations in the coding region of GCH-I gene.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
GTP cyclohydrolase 1P30793Details