Expanding the clinical and genetic spectrum of Heimler syndrome.
Feng-Juan GaoFang-Yuan HuPing XuYu-He QiJian-Kang LiYong-Jin ZhangFang ChenQing ChangFang SongSi-Mai ShenGe-Zhi XuFeng-Juan GaoPublished in: Orphanet journal of rare diseases (2019)
Next-generation sequencing is important for the diagnosis of HS. This study expands the clinical and genetic spectrum of HS, and provides additional insights into genotype-phenotype correlations, which is vital for accurate clinical practice, genetic counseling, and pathogenesis studies.