,SUFU

Joshua Aron1, Mikel Muse, Blair Harris

  • 1Corewell Health, Farmington Hills Dermatology Residency.

PubMed
概括

戈林综合征是一种罕见的遗传疾病,通常涉及修补1基因的突变. 一种罕见的融合基因突变变体抑制剂需要不同的治疗策略,包括伊特拉可纳.

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