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