MYRF Mutation Links Coronary Anomaly and Sex Disorder
Unraveling the Mysteries of MYRF Gene Mutation: A Unique Case of Coronary Artery Anomaly and 46,XY Sex Development Disorder In ...
Unraveling the Mysteries of MYRF Gene Mutation: A Unique Case of Coronary Artery Anomaly and 46,XY Sex Development Disorder In ...
Cytochrome P450 oxidoreductase deficiency (CYPOR deficiency) is an intriguing and complex genetic disorder that has recently gained attention due to ...
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