HuGE Literature Finder
Records 1 - 2
| Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes.
Psychiatry and clinical neurosciences 2018 10 73 (1): 11-19.
Ganesh Suhas, Ahmed P Husayn, Nadella Ravi K, More Ravi P, Seshadri Manasa, Viswanath Biju, Rao Mahendra, Jain Sanjeev, , Mukherjee Odi
| Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia.
Clinical genetics 2016 Apr .
Barresi S, Niceta M, Alfieri P, Brankovich V, Piccini G, Bruselles A, Barone M R, Cusmai R, Tartaglia M, Bertini E, Zanni
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