Homo sapiens RNA-seq counts of MORC2p.S87L mutation patient-derived iPSCs. Homo sapiens
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA936410
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资源简介：
MORC2 mutations can lead more severe SMA-like phenotype and CMT2Z. Through patient-derived iPSCs and MNPs, RNA-seq was performed to investigate the potential pathogenic pathways in three groups, including healthy control (HC), Spinal Muscular Atrophy-like group (SMA-like) and Charcot-Marie-Tooth disease group (CMT2Z).
创建时间：
2023-02-18
