TY  - GEN
AU  - Varon,R
AU  - Vissinga,C
AU  - Platzer,M
AU  - Cerosaletti,K M
AU  - Chrzanowska,K H
AU  - Saar,K
AU  - Beckmann,G
AU  - Seemanová,E
AU  - Cooper,P R
AU  - Nowak,N J
AU  - Stumm,M
AU  - Weemaes,C M
AU  - Gatti,R A
AU  - Wilson,R K
AU  - Digweed,M
AU  - Rosenthal,A
AU  - Sperling,K
AU  - Concannon,P
AU  - Reis,A
TI  - Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
SN  - 0092-8674
PY  - 1998///0529
KW  - Amino Acid Sequence
KW  - Base Sequence
KW  - Cell Cycle Proteins
KW  - genetics
KW  - Chromosome Aberrations
KW  - Chromosome Breakage
KW  - Chromosome Disorders
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 8
KW  - Cloning, Molecular
KW  - methods
KW  - DNA Damage
KW  - DNA Repair
KW  - Female
KW  - Founder Effect
KW  - Genes, Recessive
KW  - Humans
KW  - Linkage Disequilibrium
KW  - Male
KW  - Microcephaly
KW  - Molecular Sequence Data
KW  - Nuclear Proteins
KW  - RNA, Messenger
KW  - analysis
KW  - Sequence Analysis, DNA
KW  - Sequence Deletion
KW  - Sequence Homology, Amino Acid
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1016/s0092-8674(00)81174-5
ER  -