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A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.

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Title: A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.
Authors: Zheng, Bixia1,2, Wang, Chunyan1,3, Seltzsam, Steve1, Schneider, Sophia1, Schierbaum, Luca1, Wu, Wilfred1, Dai, Rufeng1, Connaughton, Dervla M.1, Nakayama, Makiko1, Mann, Nina1, Bauer, Stuart B.4, Awad, Hazem S.5, Eid, Loai A.5, Tasic, Velibor6, Shril, Shirlee1, Hildebrandt, Friedhelm1, friedhelm.hildebrandt@childrens.harvard.edu
Source: American Journal of Medical Genetics. Part A; Jan2022, Vol. 188 Issue 1, p310-313, 4p
Database: Applied Science & Technology Source
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DbLabel: Applied Science & Technology Source
An: 154221625
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
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  Data: A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.
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  Data: <searchLink fieldCode="JN" term="%22American+Journal+of+Medical+Genetics%2E+Part+A%22">American Journal of Medical Genetics. Part A</searchLink>; Jan2022, Vol. 188 Issue 1, p310-313, 4p
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=aci&AN=154221625
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        Value: 10.1002/ajmg.a.62502
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      – Code: eng
        Text: English
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        PageCount: 4
        StartPage: 310
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      – TitleFull: A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.
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              Text: Jan2022
              Type: published
              Y: 2022
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              Value: 188
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            – TitleFull: American Journal of Medical Genetics. Part A
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