Regional chromosomal localization of the human gene for galactose-1-phosphate uridyltransferase
Original Investigations
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Summary
In the progeny of somatic cell hybrids formed by fusion of human lymphocytes and Chinese hamster mutant cells, a single human chromosome A2 was selectively retained when grown in appropriate medium.
Spontaneous breakage of this chromosome in different hybrid subclones led to the assignment of the gene for galactose-1-phosphate uridyltransferase to the centromeric region of this chromosome (2q11-2q14). This gene is shown to be syntenic to the previously mapped genes for acid phosphatase 1 and malate dehydrogenase 1.
Keywords
Internal Medicine Metabolic Disease Somatic Cell Acid Phosphatase Human Gene
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References
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