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Successful pregnancy in a patient with mitochondrial cardiomyopathy due to ACAD9 deficiency
Acyl‐CoA dehydrogenase family member 9 (ACAD9) is an enzyme essential for the assembly of mitochondrial respiratory chain complex I. ACAD9 deficiency can cause lactic acidosis, myopathy, cardiomyopathy, intellectual disability, and early demise. We present a patient with mitochondrial myopathy, hype...
שמור ב:
| הוצא לאור ב: | JIMD Rep |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
John Wiley & Sons, Inc.
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7653261/ https://ncbi.nlm.nih.gov/pubmed/33204590 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jmd2.12157 |
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