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Annals of Indian Academy of Neurology ¦ Volume 24 ¦ Issue 4 ¦ July-August 2021 632 phenotype, rare missense variants in RELN were identified. RELN mutations segregate in an autosomal… Click to show full abstract
Annals of Indian Academy of Neurology ¦ Volume 24 ¦ Issue 4 ¦ July-August 2021 632 phenotype, rare missense variants in RELN were identified. RELN mutations segregate in an autosomal dominant fashion and the product reelin is a large secreted glycoprotein that plays essential roles in the cytoarchitecture of laminated brain structures. RELN mutation-positive patients have a higher age at onset and a milder course of disease compared to epsilon sarcoglycan M-D patients though psychiatric abnormalities and response to alcohol were common among both.[8]
Journal Title: Annals of Indian Academy of Neurology
Year Published: 2021
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