TY  - GEN
AU  - Piton,Amélie
AU  - Poquet,Hélène
AU  - Redin,Claire
AU  - Masurel,Alice
AU  - Lauer,Julia
AU  - Muller,Jean
AU  - Thevenon,Julien
AU  - Herenger,Yvan
AU  - Chancenotte,Sophie
AU  - Bonnet,Marlène
AU  - Pinoit,Jean-Michel
AU  - Huet,Frédéric
AU  - Thauvin-Robinet,Christel
AU  - Jaeger,Anne-Sophie
AU  - Le Gras,Stéphanie
AU  - Jost,Bernard
AU  - Gérard,Bénédicte
AU  - Peoc'h,Katell
AU  - Launay,Jean-Marie
AU  - Faivre,Laurence
AU  - Mandel,Jean-Louis
TI  - 20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition
SN  - 1476-5438
PY  - 2015///0206
KW  - Amino Acid Sequence
KW  - Attention Deficit and Disruptive Behavior Disorders
KW  - genetics
KW  - Base Sequence
KW  - Child Development Disorders, Pervasive
KW  - Family Health
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - High-Throughput Nucleotide Sequencing
KW  - methods
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Models, Molecular
KW  - Monoamine Oxidase
KW  - chemistry
KW  - Mutation, Missense
KW  - Pedigree
KW  - Protein Structure, Tertiary
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ejhg.2013.243
ER  -