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Dual Diagnosis of Fragile X Syndrome and DEPDC5‐Related Disorder Emphasizes DEPDC5's Role Beyond Familial Epilepsy: A Case Report and Literature Review.

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Title: Dual Diagnosis of Fragile X Syndrome and DEPDC5‐Related Disorder Emphasizes DEPDC5's Role Beyond Familial Epilepsy: A Case Report and Literature Review.
Authors: Edwards, Rory1 (AUTHOR), Murphy, Grace1 (AUTHOR), Owens, Joshua W.2,3 (AUTHOR) owensjw@upmc.edu, Erickson, Craig4 (AUTHOR), Hopkin, Robert2,3 (AUTHOR), Shillington, Amelle2,3 (AUTHOR), Das, Sofia Priyadarsani (AUTHOR)
Source: Case Reports in Genetics. 4/2/2025, Vol. 2025, p1-5. 5p.
Database: Academic Search Ultimate
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An: 184574003
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PubType: Academic Journal
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  Data: Dual Diagnosis of Fragile X Syndrome and DEPDC5‐Related Disorder Emphasizes DEPDC5's Role Beyond Familial Epilepsy: A Case Report and Literature Review.
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  Data: <searchLink fieldCode="JN" term="%22Case+Reports+in+Genetics%22">Case Reports in Genetics</searchLink>. 4/2/2025, Vol. 2025, p1-5. 5p.
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        Value: 10.1155/crig/4501466
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      – Code: eng
        Text: English
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        PageCount: 5
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      – TitleFull: Dual Diagnosis of Fragile X Syndrome and DEPDC5‐Related Disorder Emphasizes DEPDC5's Role Beyond Familial Epilepsy: A Case Report and Literature Review.
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            NameFull: Edwards, Rory
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            NameFull: Murphy, Grace
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            NameFull: Owens, Joshua W.
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            NameFull: Shillington, Amelle
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            NameFull: Das, Sofia Priyadarsani
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            – D: 02
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              Text: 4/2/2025
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              Y: 2025
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              Value: 2025
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            – TitleFull: Case Reports in Genetics
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