Literature DB >> 19018781

Uncommon MEN2A phenotype in a patient with a RET protooncogene exon 10, codon 611 mutation.

Peter Igaz, Attila Patócs, Károly Rácz.   

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Year:  2009        PMID： 19018781     DOI： 10.1111/j.1365-2265.2008.03475.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN： 0300-0664            Impact factor:   3.478


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  1 in total

1.  Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome.

Authors:  Attila Patócs; Nikoletta K Lendvai; Henriett Butz; Istvan Liko; Zoltan Sapi; Nikolette Szucs; Geza Toth; Vince K Grolmusz; Peter Igaz; Miklos Toth; Károly Rácz
Journal:  Pathol Oncol Res       Date:  2016-03-09       Impact factor: 3.201
  1 in total

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