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Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.

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Title: Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.
Authors: Ghanei, Mahmoud1,2, Sadat Fatemi, Seyedeh Helia1,2, Soudyab, Mohammad1, Esfehani, Reza Jafarzadeh2 drrezajafarzadeh@yahoo.com
Source: Neurology Asia. 2022, Vol. 27 Issue 4, p955-962. 8p.
Database: Academic Search Ultimate
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  Data: Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.
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  Data: <searchLink fieldCode="AR" term="%22Ghanei%2C+Mahmoud%22">Ghanei, Mahmoud</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Sadat+Fatemi%2C+Seyedeh+Helia%22">Sadat Fatemi, Seyedeh Helia</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Soudyab%2C+Mohammad%22">Soudyab, Mohammad</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Esfehani%2C+Reza+Jafarzadeh%22">Esfehani, Reza Jafarzadeh</searchLink><relatesTo>2</relatesTo><i> drrezajafarzadeh@yahoo.com</i>
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  Data: <searchLink fieldCode="JN" term="%22Neurology+Asia%22">Neurology Asia</searchLink>. 2022, Vol. 27 Issue 4, p955-962. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=161021111
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        Value: 10.54029/2022jdc
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      – Code: eng
        Text: English
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      – TitleFull: Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.
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            NameFull: Ghanei, Mahmoud
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            NameFull: Sadat Fatemi, Seyedeh Helia
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            NameFull: Soudyab, Mohammad
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              Text: 2022
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              Value: 27
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