טוען...
A novel composition of two heterozygous GFM1 mutations in a Chinese child with epilepsy and mental retardation
INTRODUCTION: G elongation factor mitochondrial 1 (GFM1) encodes one of the mitochondrial translation elongation factors. GFM1 variants were reported to be associated with neurological diseases and liver diseases in a few cases. Here, we present a novel composition of two heterozygous mutations of G...
שמור ב:
| הוצא לאור ב: | Brain Behav |
|---|---|
| Main Authors: | , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
John Wiley and Sons Inc.
2020
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7559602/ https://ncbi.nlm.nih.gov/pubmed/32776492 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/brb3.1791 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|