Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.

Saved in:
Bibliographic Details
Title: Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
Authors: Addis L; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; Neuroscience Discovery Research, Eli Lilly and Company, Erl Wood, Surrey, UK., Ahn JW; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK., Dobson R; Department of Biostatistics and NIHR BRC for Mental Health, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK., Dixit A; Department of Biostatistics and NIHR BRC for Mental Health, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK., Ogilvie CM; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK., Pinto D; Departments of Psychiatry, and Genetics and Genomic Sciences, Seaver Autism Center, The Mindich Child Health & Development Institute, Icahn School of Medicine at Mount Sinai, New York, New York., Vaags AK; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada., Coon H; Department of Psychiatry, University of Utah School of Medicine, Salt Lake City, Utah., Chaste P; Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania., Wilson S; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.; School of Medicine and Pharmacology, University of Western Australia, Nedlands, Western Australia, Australia., Parr JR; Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK., Andrieux J; Institut de Génétique Médicale, Hopital Jeanne de Flandre, CHRU de Lille, France., Lenne B; Centre de Génétique Chromosomique, GHICL, Hôpital Saint Vincent de Paul, Lille, France., Tumer Z; Applied Human Molecular Genetics, Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark., Leuzzi V; Department of Pediatrics, Child Neurology and Psychiatry, Sapienza Università di Roma, Rome, Italy., Aubell K; Institute of Human Genetics, Medical University of Graz, Graz, Austria., Koillinen H; Department of Clinical Genetics, Helsinki University Hospital, Helsinki, Finland., Curran S; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK., Marshall CR; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada., Scherer SW; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.; McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada., Strug LJ; Program in Genetics and Genome Biology, The Hospital for Sick Children, Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada., Collier DA; Neuroscience Discovery Research, Eli Lilly and Company, Erl Wood, Surrey, UK.; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK., Pal DK; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Source: Human mutation [Hum Mutat] 2015 Sep; Vol. 36 (9), pp. 842-50. Date of Electronic Publication: 2015 Jun 30.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1098-1004
DOI:10.1002/humu.22816