Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domain.
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| Description | scientific article |
| Author/s |
author: Nafees Ahmad Aslihan Tolun Sajid Malik |
| Publication date | June 21, 2017 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |