Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027));TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities

American Journal of Human Genetics

Volumn 93, Issue 2, 2013, Pages 197-210

  Wiszniewski, Wojciech ^a   Hunter, Jill V ^b   Hanchard, Neil A ^a,b   Willer, Jason R ^c   Shaw, Chad ^a   Tian, Qi ^a   Illner, Anna ^b   Wang, Xueqing ^a   Cheung, Sau W ^a   Patel, Ankita ^a   Campbell, Ian M ^a   Gelowani, Violet ^a   Hixson, Patricia ^a   Ester, Audrey R ^a   Azamian, Mahshid S ^a   Potocki, Lorraine ^a   Zapata, Gladys ^a   Hernandez, Patricia P ^a   Ramocki, Melissa B ^a   Santos Cortez, Regie L P ^a   Wang, Gao ^a   York, Michele K ^a   Justice, Monica J ^a   Chu, Zili D ^b   Bader, Patricia I ^d   Omo Griffith, Lisa ^d   Madduri, Nirupama S ^e   Scharer, Gunter ^f   Crawford, Heather P ^a   Yanatatsaneejit, Pattamawadee ^g   Eifert, Anna ^b   Kerr, Jeffery ^h   Bacino, Carlos A ^a   Franklin, Adiaha I A ^b   Goin Kochel, Robin P ^b   Simpson, Gayle ⁱ   Immken, Ladonna ⁱ   Haque, Muhammad E ^a   Stosic, Marija ^a   Williams, Misti D ^e   Morgan, Thomas M ^e   Pruthi, Sumit ^e   Omary, Reed ^e   Boyadjiev, Simeon A ^j   Win, Kay K ^k   Thida, Aye ^l   Hurles, Matthew ^m   Hibberd, Martin Lloyd ⁿ   Khor, Chiea Chuen ⁿ   Van Vinh Chau, Nguyen ^o   Gallagher, Thomas E ^p   Mutirangura, Apiwat ^g   Stankiewicz, Pawel ^a   Beaudet, Arthur L ^a   Maletic Savatic, Mirjana ^a   Rosenfeld, Jill A ^q   Shaffer, Lisa G ^r   Davis, Erica E ^a   Belmont, John W ^a   Dunstan, Sarah ^s   Simmons, Cameron P ^s   Bonnen, Penelope E ^a   Leal, Suzanne M ^a   Katsanis, Nicholas ^c   Lupski, James R ^a,b   Lalani, Seema R ^a   more..

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b TEXAS CHILDREN S HOSPITAL   (United States)

^c DUKE UNIVERSITY MEDICAL CENTER   (United States)

^d Northeast Indiana Genetic Counseling Center   (United States)

^e VANDERBILT UNIVERSITY   (United States)

^f CHILDREN S HOSPITAL COLORADO   (United States)

^g CHULALONGKORN UNIVERSITY   (Thailand)

^h UTHealth Austin Dell Children's Medical Center   (United States)

ⁱ Specially for Children   (United States)

^j UNIVERSITY OF CALIFORNIA   (United States)

^k HARLEM HOSPITAL CENTER   (United States)

^l Allcare Pediatrics   (United States)

^m WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

ⁿ GENOME INSTITUTE OF SINGAPORE   (Singapore)

^o UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

^p TRIPLER ARMY MEDICAL CENTER   (United States)

^q PERKINELMER INC   (United States)

^r Clinical Research Unit ^*  (United States)

^s OXFORD UNIVERSITY CLINICAL RESEARCH UNIT   (Viet Nam)

more..

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; MEMBRANE PROTEIN; TM4SF20 PROTEIN; UNCLASSIFIED DRUG;

AGING; ARTICLE; BRAIN DISEASE; CELL STRAIN HEK293; CHILD; CYTOPLASM; EXON; GENE DELETION; GENE FREQUENCY; GENE REARRANGEMENT; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; HUMAN CELL CULTURE; LANGUAGE DELAY; LINKAGE ANALYSIS; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RNA SPLICING; SCHOOL CHILD; SOUTHEAST ASIA; WHITE MATTER HYPERINTENSITY;

EID: 84881663286     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2013.07.001     Document Type: Erratum

References (29)

1. A. Ylikoski, T. Erkinjuntti, R. Raininko, S. Sarna, R. Sulkava, and R. Tilvis White matter hyperintensities on MRI in the neurologically nondiseased elderly. Analysis of cohorts of consecutive subjects aged 55 to 85 years living at home Stroke 26 1995 1171 1177
2. S. Debette, and H.S. Markus The clinical importance of white matter hyperintensities on brain magnetic resonance imaging: systematic review and meta-analysis BMJ 341 2010 c3666
3. R.O. Hopkins, C.J. Beck, D.L. Burnett, L.K. Weaver, J. Victoroff, and E.D. Bigler Prevalence of white matter hyperintensities in a young healthy population J. Neuroimaging 16 2006 243 251
4. G.L. Katzman, A.P. Dagher, and N.J. Patronas Incidental findings on brain magnetic resonance imaging from 1000 asymptomatic volunteers JAMA 282 1999 36 39
5. B.S. Kim, J. Illes, R.T. Kaplan, A. Reiss, and S.W. Atlas Incidental findings on pediatric MR images of the brain AJNR Am. J. Neuroradiol. 23 2002 1674 1677
6. E. Muscal, E. Traipe, M.M. de Guzman, B.L. Myones, R.L. Brey, and J.V. Hunter Cerebral and cerebellar volume loss in children and adolescents with systemic lupus erythematosus: a review of clinically acquired brain magnetic resonance imaging J. Rheumatol. 37 2010 1768 1775
7. F. Decobert, S. Grabar, V. Merzoug, G. Kalifa, G. Ponsot, C. Adamsbaum, and V. des Portes Unexplained mental retardation: is brain MRI useful? Pediatr. Radiol. 35 2005 587 596
8. K.T. Verbruggen, L.C. Meiners, P.E. Sijens, R.J. Lunsing, F.J. van Spronsen, and O.F. Brouwer Magnetic resonance imaging and proton magnetic resonance spectroscopy of the brain in the diagnostic evaluation of developmental delay Eur. J. Paediatr. Neurol. 13 2009 181 190
9. E. Widjaja, D. Nilsson, S. Blaser, and C. Raybaud White matter abnormalities in children with idiopathic developmental delay Acta Radiol. 49 2008 589 595
10. S.A. Back Perinatal white matter injury: the changing spectrum of pathology and emerging insights into pathogenetic mechanisms Ment. Retard. Dev. Disabil. Res. Rev. 12 2006 129 140
11. S.N. Gupta, and B. Belay Intracranial incidental findings on brain MR images in a pediatric neurology practice: a retrospective study J. Neurol. Sci. 264 2008 34 37
12. A.J. Kalnin, P.S. Fastenau, T.J. deGrauw, B.S. Musick, S.M. Perkins, C.S. Johnson, V.P. Mathews, J.C. Egelhoff, D.W. Dunn, and J.K. Austin Magnetic resonance imaging findings in children with a first recognized seizure Pediatr. Neurol. 39 2008 404 414
13. M. Kieslich, G. Errázuriz, H.G. Posselt, W. Moeller-Hartmann, F. Zanella, and H. Boehles Brain white-matter lesions in celiac disease: a prospective study of 75 diet-treated patients Pediatrics 108 2001 E21
14. P.M. Boone, C.A. Bacino, C.A. Shaw, P.A. Eng, P.M. Hixson, A.N. Pursley, S.H. Kang, Y. Yang, J. Wiszniewska, and B.A. Nowakowska Detection of clinically relevant exonic copy-number changes by array CGH Hum. Mutat. 31 2010 1326 1342
15. A.W. El-Hattab, T.A. Smolarek, M.E. Walker, E.K. Schorry, L.L. Immken, G. Patel, M.A. Abbott, B.C. Lanpher, Z. Ou, and S.H. Kang Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping Hum. Genet. 126 2009 589 602
16. A.B. Olshen, E.S. Venkatraman, R. Lucito, and M. Wigler Circular binary segmentation for the analysis of array-based DNA copy number data Biostatistics 5 2004 557 572
17. R.W. Cottingham Jr., R.M. Idury, and A.A. Schäffer Faster sequential genetic linkage computations Am. J. Hum. Genet. 53 1993 252 263
18. C.C. Khor, T.N. Chau, J. Pang, S. Davila, H.T. Long, R.T. Ong, S.J. Dunstan, B. Wills, J. Farrar, and T. Van Tram Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1 Nat. Genet. 43 2011 1139 1141
19. L. Rescorla, J. Roberts, and K. Dahlsgaard Late talkers at 2: outcome at age 3 J. Speech Lang. Hear. Res. 40 1997 556 566
20. G.R. Abecasis, D.L. Altshuler, A. Auton, L.D. Brooks, R.M. Durbin, R.A. Gibbs, M.E. Hurles, G.A. McVean 1000 Genomes Project Consortium A map of human genome variation from population-scale sequencing Nature 467 2010 1061 1073
21. S.C. Shih, A. Zukauskas, D. Li, G. Liu, L.H. Ang, J.A. Nagy, L.F. Brown, and H.F. Dvorak The L6 protein TM4SF1 is critical for endothelial cell function and tumor angiogenesis Cancer Res. 69 2009 3272 3277
22. F. Berditchevski Complexes of tetraspanins with integrins: more than meets the eye J. Cell Sci. 114 2001 4143 4151
23. S. Choi, S.A. Lee, T.K. Kwak, H.J. Kim, M.J. Lee, S.K. Ye, S.H. Kim, S. Kim, and J.W. Lee Cooperation between integrin alpha5 and tetraspan TM4SF5 regulates VEGF-mediated angiogenic activity Blood 113 2009 1845 1855
24. C.S. Lai, S.E. Fisher, J.A. Hurst, F. Vargha-Khadem, and A.P. Monaco A forkhead-domain gene is mutated in a severe speech and language disorder Nature 413 2001 519 523
25. C. Kang, and D. Drayna Genetics of speech and language disorders Annu. Rev. Genomics Hum. Genet. 12 2011 145 164
26. J.B. Tomblin, N.L. Records, P. Buckwalter, X. Zhang, E. Smith, and M. O'Brien Prevalence of specific language impairment in kindergarten children J. Speech Lang. Hear. Res. 40 1997 1245 1260
27. D. Randall, J. Reynell, and M. Curwen A study of language development in a sample of 3 year old children Br. J. Disord. Commun. 9 1974 3 16
28. B. Prathanee, S.C. Purdy, B. Thinkhamrop, B. Chaimay, N. Ruangdaraganon, L. Mo-suwan, and R. Phuphaibul Early language delay and predictive factors in children aged 2 years J. Med. Assoc. Thai. 92 2009 930 938
29. T. Tang, L. Li, J. Tang, Y. Li, W.Y. Lin, F. Martin, D. Grant, M. Solloway, L. Parker, and W. Ye A mouse knockout library for secreted and transmembrane proteins Nat. Biotechnol. 28 2010 749 755