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Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_883048509

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

Alberto Cascón, Mercedes Robledo and colleagues show that
MAX
germline mutations confer susceptibility to hereditary pheochromocytoma. This finding supports a key role for MAX and its interaction partners in tumors of neural crest cell origin.
Hereditary pheochromocytoma (PCC) is often caused by germline mutations in one of nine susceptibi...

Alternative Titles

Full title

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_883048509

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_883048509

Other Identifiers

ISSN

1061-4036

E-ISSN

1546-1718

DOI

10.1038/ng.861

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