Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73
We describe a novel nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum among 30 children (ages 1.0 to 28 years) from diverse Amish demes. Children with nephrocerebellar syndrome had progressive microcephaly, visual impairment, stagnant psychomotor development, abnormal extrapyramidal...
Main Authors: | Jinks, R.N (Author), Puffenberger, E.G (Author), Baple, E. (Author), Harding, B. (Author), Crino, P. (Author), Fogo, A.B (Author), Wenger, O. (Author), Xin, B. (Author), Koehler, A.E (Author), McGlincy, M.H (Author), Provencher, M.M (Author), Smith, J.D (Author), Tran, L. (Author), Al Turki, S. (Author), Chioza, B. A. (Author), Cross, H. (Author), Harlalka, G. V. (Author), Hurles, M. E. (Author), Maroofian, R. (Author), Heaps, A. D. (Author), Morton, M. C. (Author), Stempak, L. (Author), Hildebrandt, F. (Author), Sadowski, C. E. (Author), Zaritsky, J. (Author), Campellone, K. (Author), Morton, D. H. (Author), Wang, H. (Author), Crosby, A. (Author), Strauss, K. A. (Author) |
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Format: | Article |
Language: | English |
Published: |
2015-08.
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Subjects: | |
Online Access: | Get fulltext |
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