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Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290
Author(s) -
Ghaffari S.R.,
Rafati M.,
Ghaffari G.,
Morra M.,
Tekin M.
Publication year - 2014
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12296
Subject(s) - intellectual disability , mutation , genetics , computational biology , computer science , biology , gene
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