Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia (Q28118506)
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English | Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia |
scientific journal article |
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Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia (English)
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Han Brunner
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Martina Živná
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Jana Sovová
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Myriam Azou
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Johan Vande Walle
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Nikhita Ajit Bolar
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Gaëlle Hayot
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Christine Van Hemelrijk
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Dorien Schepers
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Geert Vandeweyer
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Ann Raes
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Erve Matthys
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Emiel Sys
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Marleen Praet
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Kelsey McFadden
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Igor Pediaditakis
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Kendrah Kidd
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Lut Van Laer
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Stanislav Kmoch
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Nicholas Katsanis
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Alexander Hoischen
Jeroen R Huyghe
Anthony J Bleyer
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