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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

PaperCitations, authors & open-access status

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 1,076 citations, 2012 year and green oa status.

1,076
Citations
2012
Year
green
OA Status

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