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Novel HIVEP2 Variants in Patients with Intellectual Disability
Intellectual disability (ID) occurs in approximately 1% of the population. Over the last years, broad sequencing approaches such as whole exome sequencing (WES) substantially contributed to the definition of the molecular defects underlying nonsyndromic ID. Pathogenic variants in HIVEP2, which encod...
שמור ב:
| הוצא לאור ב: | Mol Syndromol |
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| Main Authors: | , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
S. Karger AG
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6738162/ https://ncbi.nlm.nih.gov/pubmed/31602191 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000499060 |
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