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Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation.

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Title: Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation.
Authors: Gong, Xue1 (AUTHOR), He, Yunru1 (AUTHOR), Lu, Guoyan1 (AUTHOR), Zhang, Yulin1 (AUTHOR), Qiu, Yu1 (AUTHOR), Qiao, Lina1 (AUTHOR), Li, Yifei1 (AUTHOR) liyfwcsh@scu.edu.cn
Source: BMC Medical Genomics. 7/8/2022, Vol. 15 Issue 1, p1-9. 9p.
Database: Academic Search Ultimate
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  Data: Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation.
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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genomics%22">BMC Medical Genomics</searchLink>. 7/8/2022, Vol. 15 Issue 1, p1-9. 9p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=157888591
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        Value: 10.1186/s12920-022-01303-y
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      – TitleFull: Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation.
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            – D: 08
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              Text: 7/8/2022
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              Y: 2022
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