Germline mutations and genotype–phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma

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dc.contributor.authorPandit, R.
dc.contributor.authorKhadilkar, K.
dc.contributor.authorSarathi, V.
dc.contributor.authorMalhotra, G.
dc.date.accessioned2018-04-02T08:45:52Z
dc.date.available2018-04-02T08:45:52Z
dc.date.issued2016
dc.description.divisionRMCen
dc.format.extent5045 bytes
dc.format.mimetypetext/html
dc.identifier.sourceEuropean Journal of Endocrinology, 2016. Vol. 175 (4): pp. 311-323en
dc.identifier.urihttp://hdl.handle.net/123456789/15939
dc.language.isoenen
dc.subjectGermline mutationsen
dc.subjectgenotype–phenotype correlationen
dc.subjectAsian Indian patientsen
dc.subjectpheochromocytomaen
dc.subjectparagangliomaen
dc.titleGermline mutations and genotype–phenotype correlation in Asian Indian patients with pheochromocytoma and paragangliomaen
dc.typeArticleen

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