TY  - GEN
AU  - Pearce,S H
AU  - Cheetham,T
AU  - Imrie,H
AU  - Vaidya,B
AU  - Barnes,N D
AU  - Bilous,R W
AU  - Carr,D
AU  - Meeran,K
AU  - Shaw,N J
AU  - Smith,C S
AU  - Toft,A D
AU  - Williams,G
AU  - Kendall-Taylor,P
TI  - A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1
SN  - 0002-9297
PY  - 1999///0201
KW  - Alleles
KW  - Base Sequence
KW  - Chromosomes, Human, Pair 21
KW  - genetics
KW  - Exons
KW  - Female
KW  - Founder Effect
KW  - Genotype
KW  - Haplotypes
KW  - Humans
KW  - Male
KW  - Molecular Sequence Data
KW  - Nuclear Family
KW  - Pedigree
KW  - Point Mutation
KW  - Polyendocrinopathies, Autoimmune
KW  - Polymorphism, Single-Stranded Conformational
KW  - Sequence Analysis, DNA
KW  - Sequence Deletion
KW  - Transcription Factors
KW  - United Kingdom
KW  - AIRE Protein
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1086/302145
ER  -