Whole-exome sequencing identifies Max mutations as a cause of hereditary pheochromocytoma. Whole-exome sequencing identifies Max mutations as a cause of hereditary pheochromocytoma

Name: Whole-exome sequencing identifies Max mutations as a cause of hereditary pheochromocytoma. Whole-exome sequencing identifies Max mutations as a cause of hereditary pheochromocytoma
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https://www.ncbi.nlm.nih.gov/bioproject/PRJEB2461

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资源简介：

Whole exome sequencing identification of Max mutations and further validation in pheochromocytoma patients

创建时间：

2012-03-01