NEMO mutation as a cause of familial occurrence of Behçet's disease in female patients.

Takada, H

NEMO mutation as a cause of familial occurrence of Behçet's disease in female patients. [electronic resource] - Clinical genetics Dec 2010 - 575-9 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1399-0004

10.1111/j.1399-0004.2010.01432.x doi


Adult
Base Sequence
Behcet Syndrome--genetics
Child
Female
Heterozygote
Humans
I-kappa B Kinase--genetics
Molecular Sequence Data
Mutation
X Chromosome Inactivation--genetics