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Range of genetic mutations associated with severe non-syn... | ResearchHub
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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
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Authors
Anita Rauch
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Anita Rauch
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Olaf Rieß
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•
Tim Strom
Published
September 27, 2012
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Journal
The Lancet
Topics
Biology
Internal Medicine
Medicine
Phenotype
Loss Function
Show all topics
DOI
10.1016/s0140-6736(12)61480-9
