Title : A patient with an apparently sporadic pheochromocytoma with a rearranged during transfection codon 635 variant: a mild form of multiple endocrine neoplasia type 2?

Pub. Date : 2014 Apr

PMID : 24449676






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 CONCLUSIONS: The majority of mutations in this disorder affect cysteine residues in the cysteine-rich region of the extracellular domain of the RET protein, disrupting normal cysteine pairing. Cysteine ret proto-oncogene Homo sapiens
2 CONCLUSIONS: The majority of mutations in this disorder affect cysteine residues in the cysteine-rich region of the extracellular domain of the RET protein, disrupting normal cysteine pairing. Cysteine ret proto-oncogene Homo sapiens
3 CONCLUSIONS: The majority of mutations in this disorder affect cysteine residues in the cysteine-rich region of the extracellular domain of the RET protein, disrupting normal cysteine pairing. Cysteine ret proto-oncogene Homo sapiens