ABOVE is the twenty-four (24) hour day of CHROMOSOMIC CLOCK and this time is one (#1). 
Here I present: “Paroxysmal Kinesigenic Choreoathetosis”, Victor McKusick, Mendelian Inheritance in Man’, 1966.
INTRODUCTION.
1. Paroxysmal Kinesigenic Choreoathetosis is a rare disorder characterized by attacks of involuntary movements, which are triggered by sudden voluntary movements. The number of attacks can increase during puberty and decrease in a person’s 20s to 30s. Involuntary movements can take many forms such as chorea or dystonia and usually only affect one side of the body or one limb in particular.
2. Paroxysmal Kinesigenic Choreoathetosis is also called Dystonia type-9 (DYT9). Dystonia-9 (DYT9) is caused by heterozygous mutation in the SLC2A1 gene on cytogenetic location 1p34.2 and genomic coordinates 1:42,925,353-42,958,868 . The screenshot of the SLC2A1 gene is shown BELOW of the 33,516 bp (base pairs) of DNA sequence length.
