Citations for
1RELN, LIS2
The role of RELN in lissencephaly and neuropsychiatric disease.
Chang BS, Duzcan F, Kim S, Cinbis M, Aggarwal A, Apse KA, Ozdel O, Atmaca M, Zencir S, Bagci H, Walsh CA.
Am J Med Genet B Neuropsychiatr Genet 144(1):58-63. 2007
2LIS2, RELN
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA.
Nat Genet 26(1):93-6. No abstract available. 2000