Parental Whole-Exome Sequencing Enables Sialidosis Type II Diagnosis due to an NEU1 Missense Mutation as an Underlying Cause of Nephrotic Syndrome in the Child

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Publication year
2018
Author(s)
Maroofian, Reza
Schuele, Isabel
Najafi, Maryam
Bakey, Z.
Rad, Abolfazi
Antony, D.
Habibi, Haleh
Schmidt, Miriam
Source
Kidney International Reports, 3, 6, (2018), pp. 1454-1463
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/197983   https://hdl.handle.net/2066/197983
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