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Volumn 34, Issue 1, 2003, Pages 27-29
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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
a a b,f c b,d c c b b,e c,f a c b d d d g h h h more.. |
Author keywords
[No Author keywords available]
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Indexed keywords
CELL ADHESION MOLECULE;
GENE PRODUCT;
NEUROLIGIN;
PROTEIN NLGN3;
PROTEIN NLGN4;
UNCLASSIFIED DRUG;
ARTICLE;
AUTISM;
CELLULAR DISTRIBUTION;
DISEASE ASSOCIATION;
DISEASE PREDISPOSITION;
FEMALE;
GENE MUTATION;
GENETIC PREDISPOSITION;
GENETIC TRANSCRIPTION;
HUMAN;
MALE;
NUCLEOTIDE SEQUENCE;
PRIORITY JOURNAL;
SEQUENCE ANALYSIS;
SEQUENCE HOMOLOGY;
SIBLING;
SYNAPSE;
SYNAPTOGENESIS;
X CHROMOSOME LINKAGE;
AMINO ACID SEQUENCE;
AUTISTIC DISORDER;
BASE SEQUENCE;
BRAIN;
CARRIER PROTEINS;
CHROMOSOMES, HUMAN, X;
DNA, COMPLEMENTARY;
FEMALE;
GENE EXPRESSION PROFILING;
HUMANS;
LINKAGE (GENETICS);
MALE;
MEMBRANE PROTEINS;
MOLECULAR SEQUENCE DATA;
MUTATION;
NERVE TISSUE PROTEINS;
PEDIGREE;
RNA, MESSENGER;
SEQUENCE HOMOLOGY, AMINO ACID;
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EID: 0037656313
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/ng1136 Document Type: Article |
Times cited : (1456)
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References (15)
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