TY  - GEN
AU  - Takada,H
AU  - Nomura,A
AU  - Ishimura,M
AU  - Ichiyama,M
AU  - Ohga,S
AU  - Hara,T
TI  - NEMO mutation as a cause of familial occurrence of Behçet's disease in female patients
SN  - 1399-0004
PY  - 2011///0222
KW  - Adult
KW  - Base Sequence
KW  - Behcet Syndrome
KW  - genetics
KW  - Child
KW  - Female
KW  - Heterozygote
KW  - Humans
KW  - I-kappa B Kinase
KW  - Molecular Sequence Data
KW  - Mutation
KW  - X Chromosome Inactivation
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1399-0004.2010.01432.x
ER  -