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A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy.

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Title: A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy.
Authors: Nejati, Parham1,2 (AUTHOR), Falsafi, Nafiseh3 (AUTHOR), Alimoradi, Elham4 (AUTHOR), Khosravi, Teymoor5,6 (AUTHOR), Kamari, Mohana1 (AUTHOR), Oladnabi, Morteza6,7 (AUTHOR) oladnabidozin@yahoo.com, Alibakhshi, Reza1,4 (AUTHOR) ralibakhshi@kums.ac.ir
Source: BMC Medical Genomics. 11/4/2025, Vol. 18 Issue 1, p1-9. 9p.
Database: Academic Search Ultimate
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An: 189086954
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  Data: A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy.
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  Data: <searchLink fieldCode="AR" term="%22Nejati%2C+Parham%22">Nejati, Parham</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Falsafi%2C+Nafiseh%22">Falsafi, Nafiseh</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Alimoradi%2C+Elham%22">Alimoradi, Elham</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Khosravi%2C+Teymoor%22">Khosravi, Teymoor</searchLink><relatesTo>5,6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kamari%2C+Mohana%22">Kamari, Mohana</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Oladnabi%2C+Morteza%22">Oladnabi, Morteza</searchLink><relatesTo>6,7</relatesTo> (AUTHOR)<i> oladnabidozin@yahoo.com</i><br /><searchLink fieldCode="AR" term="%22Alibakhshi%2C+Reza%22">Alibakhshi, Reza</searchLink><relatesTo>1,4</relatesTo> (AUTHOR)<i> ralibakhshi@kums.ac.ir</i>
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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genomics%22">BMC Medical Genomics</searchLink>. 11/4/2025, Vol. 18 Issue 1, p1-9. 9p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=189086954
RecordInfo BibRecord:
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    Identifiers:
      – Type: doi
        Value: 10.1186/s12920-025-02254-w
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      – Code: eng
        Text: English
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        PageCount: 9
        StartPage: 1
    Titles:
      – TitleFull: A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy.
        Type: main
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          Name:
            NameFull: Nejati, Parham
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            NameFull: Falsafi, Nafiseh
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            NameFull: Alimoradi, Elham
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            NameFull: Khosravi, Teymoor
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            NameFull: Kamari, Mohana
      – PersonEntity:
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            NameFull: Oladnabi, Morteza
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            NameFull: Alibakhshi, Reza
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          Dates:
            – D: 04
              M: 11
              Text: 11/4/2025
              Type: published
              Y: 2025
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            – TitleFull: BMC Medical Genomics
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