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Familial neurofibromatosis type 1 has diverse manifestations in skin and is associated with steatocystoma multiplex
Author(s) -
Zhang Y.,
Fang M.,
Ding X.,
Tang L.,
Zhang X.
Publication year - 2021
Publication title -
clinical and experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 78
eISSN - 1365-2230
pISSN - 0307-6938
DOI - 10.1111/ced.14618
Subject(s) - multiplex , type (biology) , dermatology , neurofibromatosis , neurofibromatosis type 2 , medicine , computer science , pathology , genetics , biology , ecology
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