TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.

Wiszniewski W, Hunter JV, Hanchard NA, Willer JR, Shaw C, Tian Q, Illner A, Wang X, Cheung SW, Patel A, Campbell IM, Gelowani V, Hixson P, Ester AR, Azamian MS, Potocki L, Zapata G, Hernandez PP, Ramocki MB, Santos-Cortez RL, Wang G, York MK, Justice MJ, Chu ZD, Bader PI, Omo-Griffith L, Madduri NS, Scharer G, Crawford HP, Yanatatsaneejit P, Eifert A, Kerr J, Bacino CA, Franklin AI, Goin-Kochel RP, Simpson G, Immken L, Haque ME, Stosic M, Williams MD, Morgan TM, Pruthi S, Omary R, Boyadjiev SA, Win KK, Thida A, Hurles M, Hibberd ML, Khor CC, Van Vinh Chau N, Gallagher TE, Mutirangura A, Stankiewicz P, Beaudet AL, Maletic-Savatic M, Rosenfeld JA, Shaffer LG, Davis EE, Belmont JW, Dunstan S, Simmons CP, Bonnen PE, Leal SM, Katsanis N, Lupski JR, Lalani SR
Am J Hum Genet. 2013 93 (2): 197-210

PMID: 23810381 · PMCID: PMC3738832 · DOI:10.1016/j.ajhg.2013.05.027

MeSH Terms (21)

Age of Onset Aging, Premature Asian Continental Ancestry Group Base Sequence Brain Child Child, Preschool Chromosomes, Human, Pair 2 Exons Female Genetic Predisposition to Disease Humans Language Development Disorders Leukoencephalopathies Magnetic Resonance Imaging Male Molecular Sequence Data Pedigree Sequence Analysis, DNA Sequence Deletion Tetraspanins

Connections (1)

This publication is referenced by other Labnodes entities:

Links