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. 1989 Dec;45(6):910-6.

Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP

M Simon  1 , M Phillips, H Green, H Stroh, K Glatt, G Burns, S A Latt
Affiliations

Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP

M Simon et al. 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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References

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