9例のインド人におけるβ‐ケトチオラーゼ欠損症の分子特性化:ACAT1遺伝子における3つの新規な突然変異の発見
openalex(2016)
AI Read Science
Must-Reading Tree
Example

Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined
openalex(2016)