Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
Top Cited Papers
- 27 September 2012
- journal article
- research article
- Published by Elsevier BV in The Lancet
- Vol. 380 (9854), 1674-1682
- https://doi.org/10.1016/s0140-6736(12)61480-9
Abstract
No abstract availableKeywords
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