Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP.
Am J Hum Genet
; 45(6): 910-6, 1989 Dec.
Article
em En
| MEDLINE
| ID: mdl-2574003
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.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Precursores de Proteínas
/
Polimorfismo de Fragmento de Restrição
/
Sequências Repetitivas de Ácido Nucleico
Limite:
Animals
/
Humans
Idioma:
En
Revista:
Am J Hum Genet
Ano de publicação:
1989
Tipo de documento:
Article
