Rett syndrome (RTT) is a progressive neurological disorder, affecting females with mutations in the X‐linked gene methyl‐CpG‐binding protein 2 (MECP2). While MECP2 has been implicated in cancers of the breast, colon, and prostrate, cancer in pat...
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https://www.riss.kr/link?id=O106845265
2021년
-
0303-6987
1600-0560
SCI;SCIE;SCOPUS
학술저널
908-910 [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
Rett syndrome (RTT) is a progressive neurological disorder, affecting females with mutations in the X‐linked gene methyl‐CpG‐binding protein 2 (MECP2). While MECP2 has been implicated in cancers of the breast, colon, and prostrate, cancer in pat...
Rett syndrome (RTT) is a progressive neurological disorder, affecting females with mutations in the X‐linked gene methyl‐CpG‐binding protein 2 (MECP2). While MECP2 has been implicated in cancers of the breast, colon, and prostrate, cancer in patients with RTT is rare. We present a case of malignant melanoma in a patient with RTT, which additionally, displayed hitherto undescribed nuclear features, resembling herpes simplex virus cytopathic effects.
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