RNAseq analysis of PL/J, MRL/MpJ and FVB/NJ using murine lung
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https://www.ncbi.nlm.nih.gov/sra/DRP005354
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资源简介：
Pulmonary arterial hypertension (PAH) is rare and eventually fatal disease. PAH patients can carry mutations commonly in BMPR2. But not all patients carry these PAH mutations. Our goal is to identify the genomic factors contributing to development of the PAH.
创建时间：
2019-08-16
