טוען...
Donor Splice-Site Mutation in CUL4B is Likely Cause of X-Linked Intellectual Disability
X-linked intellectual disability is the most common form of cognitive disability in males. Syndromic intellectual disability encompasses cognitive deficits with other medical and behavioral manifestations. Recently, a large family with a novel form of syndromic X-linked intellectual disability was c...
שמור ב:
| הוצא לאור ב: | Am J Med Genet A |
|---|---|
| Main Authors: | , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2014
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4404493/ https://ncbi.nlm.nih.gov/pubmed/24898194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.36629 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|