Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma - Concepedia

Concepedia

Publication | Open Access

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

DOI Full Paper Access

524

Citations

35

References

2011

Year

Iñaki Comino‐Méndez, Francisco Javier Gracia-Aznárez, Francesca Schiavi, Iñigo Landa, Luis J. Leandro‐García, Rocío Letón, Emiliano Honrado, Rocío Ramos‐Medina, Daniela Caronia, Guillermo Pita,

Nature Genetics

Hereditary PheochromocytomaMendelian DisorderGenetic DisorderMedicineGeneticsPathologyMolecular GeneticsIdentifies Max MutationsGenomicsDisease Gene IdentificationMolecular DiagnosticsVariant Interpretation

References

	Year	Citations

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