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Journal description
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Details for article 8 of 22 found articles
| Title: |
De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome |
| Author: |
Palmer, Elizabeth E. Hong, Seungbeom Al Zahrani, Fatema Hashem, Mais O. Aleisa, Fajr A. Jalal Ahmed, Heba M. Kandula, Tejaswi Macintosh, Rebecca Minoche, Andre E. Puttick, Clare Gayevskiy, Velimir Drew, Alexander P. Cowley, Mark J. Dinger, Marcel Rosenfeld, Jill A. Xiao, Rui Cho, Megan T. Yakubu, Suliat F. Henderson, Lindsay B. Guillen Sacoto, Maria J. Begtrup, Amber Hamad, Muddathir Shinawi, Marwan Andrews, Marisa V. Jones, Marilyn C. Lindstrom, Kristin Bristol, Ruth E. Kayani, Saima Snyder, Molly Villanueva, Marıá Mercedes Schteinschnaider, Angeles Faivre, Laurence Thauvin, Christel Vitobello, Antonio Roscioli, Tony Kirk, Edwin P. Bye, Ann Merzaban, Jasmeen Jaremko, Łukasz Jaremko, Mariusz Sachdev, Rani K. Alkuraya, Fowzan S. Arold, Stefan T. |
| Appeared in: |
The American journal of human genetics |
| Paging: | Volume 104 (2019) nr. 4 pages 778 |
| Year: |
2019 |
| Contents: | |
| Publisher: |
American Society of Human Genetics |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 8 of 22 found articles
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