TY  - GEN
AU  - Duong,Linh
AU  - Klitten,Laura L
AU  - Møller,Rikke S
AU  - Ingason,Andrés
AU  - Jakobsen,Klaus D
AU  - Skjødt,Celina
AU  - Didriksen,Michael
AU  - Hjalgrim,Helle
AU  - Werge,Thomas
AU  - Tommerup,Niels
TI  - Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders
SN  - 1552-485X
PY  - 2012///1005
KW  - Adult
KW  - Aged
KW  - Base Sequence
KW  - Brain Diseases
KW  - genetics
KW  - Calcium-Binding Proteins
KW  - Cell Adhesion Molecules, Neuronal
KW  - Child
KW  - Child, Preschool
KW  - DNA Mutational Analysis
KW  - Exons
KW  - Family
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Introns
KW  - Male
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - Neural Cell Adhesion Molecules
KW  - Pedigree
KW  - Phenotype
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.b.32036
ER  -