Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: GABARAPL1[original query] |
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Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human molecular genetics 2012 Aug 21 (15): 3513-23. Griswold Anthony J, Ma Deqiong, Cukier Holly N, Nations Laura D, Schmidt Mike A, Chung Ren-Hua, Jaworski James M, Salyakina Daria, Konidari Ioanna, Whitehead Patrice L, Wright Harry H, Abramson Ruth K, Williams Scott M, Menon Ramkumar, Martin Eden R, Haines Jonathan L, Gilbert John R, Cuccaro Michael L, Pericak-Vance Margaret |
Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment. NPJ genomic medicine 2023 2 8 (1): 4. Morimoto Marie, Bhambhani Vikas, Gazzaz Nour, Davids Mariska, Sathiyaseelan Paalini, Macnamara Ellen F, Lange Jennifer, Lehman Anna, Zerfas Patricia M, Murphy Jennifer L, Acosta Maria T, Wang Camille, Alderman Emily, , Reichert Sara, Thurm Audrey, Adams David R, Introne Wendy J, Gorski Sharon M, Boerkoel Cornelius F, Gahl William A, Tifft Cynthia J, Malicdan May Christine |
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