Identification of NF1 Frameshift Variants in Two Chinese Families With Neurofibromatosis Type 1 and Early-Onset Hypertension

Background: Neurofibromatosis type 1 (NF-1) is a common autosomal dominant disorder caused by mutations in the NF1 gene. It is characterized by multiple café-au-lait macules, cutaneous neurofibromas, optic glioma, Lisch nodules, and axillary and inguinal freckling. The aim of this study was to inve...

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Main Authors: Yi-Ting Lu (Author), Di Zhang (Author), Xin-Chang Liu (Author), Qiong-Yu Zhang (Author), Xue-Qi Dong (Author), Peng Fan (Author), Yan Xiao (Author), Xian-Liang Zhou (Author)
Format: Book
Published: Frontiers Media S.A., 2021-12-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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