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Journal description
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Details for article 27 of 47 found articles
| Title: |
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α1 subunit of the inhibitory glycine receptor |
| Author: |
Rees, Mark I. Andrew, Martin Jawad, Sudad Owen, Michael J. |
| Appeared in: |
Human molecular genetics |
| Paging: | Volume 3 (1994) nr. 12 pages 2175-2179 |
| Year: |
1994-12 |
| Contents: | |
| Publisher: |
Oxford University Press, Oxford |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 27 of 47 found articles
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