Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation

American Journal of Human Genetics

Volumn 75, Issue 2, 2004, Pages 318-324

  Tarpey, Patrick ^a   Parnau, Josep ^b   Blow, Matthew ^a   Woffendin, Hayley ^a   Bignell, Graham ^a   Cox, Charles ^a   Cox, James ^b   Davies, Helen ^a   Edkins, Sarah ^a   Holden, Simon ^b   Korny, Angelique ^a   Mallya, Uma ^b   Moon, Jenny ^b   O'Meara, Sarah ^a   Parker, Adrian ^a   Stephens, Philip ^a   Stevens, Claire ^a   Teague, Jon ^a   Donnelly, Andrew ^d,e   Mangelsdorf, Marie ^d,e   Mulley, John ^d,e   Partington, Michael ^f,g   Turner, Gillian ^f,g   Stevenson, Roger ^h   Schwartz, Charles ^h   Young, Ian ⁱ   Easton, Douglas ^c   Bobrow, Martin ^b   Futreal, P Andrew ^a   Stratton, Michael R ^a   Gecz, Jozef ^d,e   Wooster, Richard ^a   Raymond, F Lucy ^b   more..

^a WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^b UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^d WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^e UNIVERSITY OF ADELAIDE   (Australia)

^f Hunter Health   (Australia)

^g UNIVERSITY OF NEWCASTLE   (Australia)

^h GREENWOOD GENETIC CENTER   (United States)

ⁱ LEICESTER ROYAL INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; GLUTAMATE RECEPTOR; GUANYLATE KINASE; MEMBRANE ENZYME; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR NR2 SUBUNIT; PDZ PROTEIN; RECEPTOR SUBUNIT; SYNAPSE ASSOCIATED PROTEIN 102; UNCLASSIFIED DRUG;

ARTICLE; BRAIN DEVELOPMENT; CARBOXY TERMINAL SEQUENCE; DLG3 GENE; FAMILY STUDY; FEMALE; GENE; GENE MUTATION; HUMAN; LEARNING; LONG TERM DEPRESSION; LONG TERM POTENTIATION; MAJOR CLINICAL STUDY; MALE; MEMORY; NERVE CELL PLASTICITY; NONSYNDROMIC X LINKED MENTAL RETARDATION; NUCLEOTIDE SEQUENCE; PDZ DOMAIN; POSTSYNAPTIC MEMBRANE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN FAMILY; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; SIGNAL TRANSDUCTION; SRC HOMOLOGY DOMAIN; STOP CODON; SYNAPSE; X LINKED MENTAL RETARDATION;

EID: 3242696203     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/422703     Document Type: Article

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