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ng.861
ng.861
https://scigraph.springernature.com/pub.10.1038/ng.861
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
P2888
Q28241168-8137FDA8-6D40-454F-B9A8-033004B31ABC
P2888
ng.861
https://scigraph.springernature.com/pub.10.1038/ng.861