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Year | Number of Results |
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1998 | 1 |
2001 | 1 |
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Calcium-dependent interaction of Lis1 with IQGAP1 and Cdc42 promotes neuronal motility.
Nat Neurosci. 2006 Jan;9(1):50-7. doi: 10.1038/nn1619. Epub 2005 Dec 20.
Nat Neurosci. 2006.
PMID: 16369480
Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations.
Ross ME, Swanson K, Dobyns WB.
Ross ME, et al.
Neuropediatrics. 2001 Oct;32(5):256-63. doi: 10.1055/s-2001-19120.
Neuropediatrics. 2001.
PMID: 11748497
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LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.
Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM, Walsh CA, Barkovich AJ, Dobyns WB, Ledbetter DH, Ross ME.
Pilz DT, et al.
Hum Mol Genet. 1998 Dec;7(13):2029-37. doi: 10.1093/hmg/7.13.2029.
Hum Mol Genet. 1998.
PMID: 9817918
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