Novel G342L MAPT mutation in familial Progressive Supranuclear Palsy Syndrome. Novel G342L MAPT mutation in familial Progressive Supranuclear Palsy Syndrome

Name: Novel G342L MAPT mutation in familial Progressive Supranuclear Palsy Syndrome. Novel G342L MAPT mutation in familial Progressive Supranuclear Palsy Syndrome
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NIAID Data Ecosystem2026-05-01 收录

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https://www.ncbi.nlm.nih.gov/bioproject/PRJEB73767

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The PSP pedigree caused by the novel MAPT (G342L) mutation, expanded the mutational spectrum of MAPT.

创建时间：

2024-03-30