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An Intron Mutation in the ACVRL1 May Be Associated with a Transcriptional Regulation Defect in a Chinese Family with Hereditary Hemorrhagic Telangiectasia
Yu Q,
Shen Xh,
Li Y,
Li Rj,
Li J,
et al.
(2013)
An Intron Mutation in the ACVRL1 May Be Associated with a Transcriptional Regulation Defect in a Chinese Family with Hereditary Hemorrhagic Telangiectasia.
PLOS ONE 8(2): e58031.
https://doi.org/10.1371/journal.pone.0058031