Whole Exome Sequencing Identifies Causative Mutations In The Majority Of Consanguineous Or Familial Cases With Childhood-Onset Increased Renal Echogenicity

Göster/Aç
Tarih
2016
Yazar
Braun, Daniela A.
Schueler, Markus
Halbritter, Jan
Gee, Heon Yung
Porath, Jonathan D.
Lawson, Jennifer A.
Airik, Rannar
Shril, Shirlee
Allen, Susan J.
Stein, Deborah
Al Kindy, Adila
Beck, Bodo B.
Cengiz, Nurcan
Moorani, Khemchand N.
Ozaltin, Fatih
Hashmi, Seema
Sayer, John A.
Bockenhauer, Detlef
Soliman, Neveen A.
Otto, Edgar A.
Lifton, Richard P.
Hildebrandt, Friedhelm
Üst veri
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Bağlantı
https://doi.org/10.1038/ki.2015.317
https://linkinghub.elsevier.com/retrieve/pii/S008525381500040X
http://hdl.handle.net/11655/14518
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