Carnitine-acylcarnitine translocase deficiency with c.199-10 T>G and novel c.1A>G mutation: Two case reports and brief literature review.
Carnitine-acylcarnitine translocase deficiency with c.199-10 T>G and novel c.1A>G mutation: Two case reports and brief literature review. — المؤلف: Yan, Hui-Ming — Medicine 20171130
- المؤلف
- Yan, Hui-Ming
- النشر
- Medicine 20171130
- الوصف
- e8549 p.
- الموضوعات
- Carnitine Acyltransferases؛ China؛ DNA Mutational Analysis؛ Fatal Outcome؛ Female؛ Founder Effect؛ Genotype؛ Humans