Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP
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- PMCID: PMC1683481
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Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP
Am J Hum Genet.
1989 Dec.
Abstract
The human involucrin gene has been mapped to the region q21-q22 of chromosome 1. Three of six Utah families examined were polymorphic for a PstI fragment of the involucrin gene. In one individual, the variant PstI fragment was found by DNA sequencing to be missing one of the 39 repeats that make up two-thirds of the coding region.
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