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Novel TTN Mutation Causing Severe Congenital Myopathy and Uncertain Association with Infantile Hydrocephalus.

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Title: Novel TTN Mutation Causing Severe Congenital Myopathy and Uncertain Association with Infantile Hydrocephalus.
Authors: Balasundaram, Palanikumar1 (AUTHOR), Avulakunta, Indirapriya Darshini1 (AUTHOR), Delfiner, Leslie2 (AUTHOR), Levy, Paul3 (AUTHOR), Forman, Katie R.1 (AUTHOR)
Source: Case Reports in Genetics. 7/18/2023, p1-4. 4p.
Database: Academic Search Ultimate
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  Data: Novel TTN Mutation Causing Severe Congenital Myopathy and Uncertain Association with Infantile Hydrocephalus.
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  Data: <searchLink fieldCode="JN" term="%22Case+Reports+in+Genetics%22">Case Reports in Genetics</searchLink>. 7/18/2023, p1-4. 4p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=165126089
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        Value: 10.1155/2023/5535083
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      – Code: eng
        Text: English
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      – TitleFull: Novel TTN Mutation Causing Severe Congenital Myopathy and Uncertain Association with Infantile Hydrocephalus.
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            NameFull: Balasundaram, Palanikumar
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            NameFull: Avulakunta, Indirapriya Darshini
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            NameFull: Delfiner, Leslie
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            NameFull: Levy, Paul
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              Text: 7/18/2023
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              Y: 2023
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