20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition. [electronic resource]
Producer: 20150206Description: 776-83 p. digitalISSN:- 1476-5438
- Amino Acid Sequence
- Attention Deficit and Disruptive Behavior Disorders -- genetics
- Base Sequence
- Child Development Disorders, Pervasive -- genetics
- Family Health
- Female
- Genetic Predisposition to Disease -- genetics
- High-Throughput Nucleotide Sequencing -- methods
- Humans
- Intellectual Disability -- genetics
- Male
- Models, Molecular
- Monoamine Oxidase -- chemistry
- Mutation, Missense
- Pedigree
- Protein Structure, Tertiary
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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