SHANK1 deletions in males with autism spectrum disorder

American Journal of Human Genetics

Volumn 90, Issue 5, 2012, Pages 879-887

  Sato, Daisuke ^a   Lionel, Anath C ^a,b   Leblond, Claire S ^c,d,e   Prasad, Aparna ^a   Pinto, Dalila ^a   Walker, Susan ^a   O'Connor, Irene ^f   Russell, Carolyn ^f   Drmic, Irene E ^g   Hamdan, Fadi F ^h   Michaud, Jacques L ^h   Endris, Volker ⁱ   Roeth, Ralph ⁱ   Delorme, Richard ^c,d,e,j   Huguet, Guillaume ^c,d,e   Leboyer, Marion ^k,l   Rastam, Maria ^m   Gillberg, Christopher ^n,o   Lathrop, Mark ^p   Stavropoulos, Dimitri J ^g   Anagnostou, Evdokia ^q   Weksberg, Rosanna ^g   Fombonne, Eric ^r   Zwaigenbaum, Lonnie ^s   Fernandez, Bridget A ^t   Roberts, Wendy ^g,q   Rappold, Gudrun A ⁱ   Marshall, Christian R ^a,b   Bourgeron, Thomas ^c,d,e   Szatmari, Peter ^f   Scherer, Stephen W ^a,b   more..

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c INSTITUT PASTEUR   (France)

^d UNIVERSITÉ PARIS DESCARTES   (France)

^e CNRS   (France)

^f MCMASTER UNIVERSITY   (Canada)

^g HOSPITAL FOR SICK CHILDREN   (Canada)

^h UNIVERSITY OF MONTREAL   (Canada)

ⁱ UNIVERSITY OF HEIDELBERG   (Germany)

^j HÔPITAL ROBERT DEBRÉ   (France)

^k INSERM U955   (France)

^l FONDATION FONDAMENTAL   (France)

^m LUND UNIVERSITY   (Sweden)

ⁿ UNIVERSITY OF GOTHENBURG   (Sweden)

^o UNIVERSITY COLLEGE LONDON   (United Kingdom)

^p CENTRE NATIONAL DE GÉNOTYPAGE   (France)

^q University of Toronto   (Canada)

^r MONTREAL CHILDREN S HOSPITAL   (Canada)

^s UNIVERSITY OF ALBERTA   (Canada)

^t MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

more..

Author keywords

[No Author keywords available]

Indexed keywords

SCAFFOLD PROTEIN; SHANK1 PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME 19; FAMILY; FEMALE; FUNCTIONAL STATUS; GENDER BIAS; GENE DELETION; GENE LOCUS; GENE MUTATION; HEMIZYGOSITY; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; PENETRANCE; PRESCHOOL CHILD; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CANADA; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; DNA COPY NUMBER VARIATIONS; EUROPE; FEMALE; HUMANS; INTELLECTUAL DISABILITY; MALE; MUTATION; NERVE TISSUE PROTEINS; NEURONS; PEDIGREE; SEQUENCE DELETION; SYNAPSES;

EID: 84860739976     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2012.03.017     Document Type: Article

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