Frequent Germ-Line Mutations of the MEN1, CASR, and HRPT2/CDC73 Genes in Young Patients with Clinically Non-familial Primary Hyperparathyroidism

Lee F. Starker; Tobias Åkerström; William D. Long; Alberto Delgado-Verdugo; Patricia Donovan; Robert Udelsman; Richard P. Lifton; Tobias Carling

doi:10.1007/s12672-011-0100-8

Frequent Germ-Line Mutations of the MEN1, CASR, and HRPT2/CDC73 Genes in Young Patients with Clinically Non-familial Primary Hyperparathyroidism

Lee F. Starker, Tobias Åkerström, William D. Long, Alberto Delgado-Verdugo, Patricia Donovan, Robert Udelsman, Richard P. Lifton, Tobias Carling

Research output: Contribution to journal › Article › peer-review

Original language	American English
Journal	Hormones and Cancer
Volume	3
DOIs	https://doi.org/10.1007/s12672-011-0100-8
State	Published - Apr 1 2012
Externally published	Yes

Disciplines

Endocrinology, Diabetes, and Metabolism
Endocrinology
Biology
Oncology
Internal Medicine

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10.1007/s12672-011-0100-8License: Unspecified

Cite this

@article{128426c1332e425b866ed38152433707,

title = "Frequent Germ-Line Mutations of the MEN1, CASR, and HRPT2/CDC73 Genes in Young Patients with Clinically Non-familial Primary Hyperparathyroidism",

author = "Starker, \{Lee F.\} and Tobias {\AA}kerstr{\"o}m and Long, \{William D.\} and Alberto Delgado-Verdugo and Patricia Donovan and Robert Udelsman and Lifton, \{Richard P.\} and Tobias Carling",

note = "Familial primary hyperparathyroidism (FPHPT) may occur due to an underlying germ-line mutation in the MEN1, CASR, or HRPT2/ CDC73 genes. The disease may be undiagnosed in the absence of a history suggestive of FHPT. Young PHPT patients (≤45 years of age) are more likely to harbor occult FPHPT.",

year = "2012",

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day = "1",

doi = "10.1007/s12672-011-0100-8",

language = "American English",

volume = "3",

journal = "Hormones and Cancer",

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TY - JOUR

T1 - Frequent Germ-Line Mutations of the MEN1, CASR, and HRPT2/CDC73 Genes in Young Patients with Clinically Non-familial Primary Hyperparathyroidism

AU - Starker, Lee F.

AU - Åkerström, Tobias

AU - Long, William D.

AU - Delgado-Verdugo, Alberto

AU - Donovan, Patricia

AU - Udelsman, Robert

AU - Lifton, Richard P.

AU - Carling, Tobias

N1 - Familial primary hyperparathyroidism (FPHPT) may occur due to an underlying germ-line mutation in the MEN1, CASR, or HRPT2/ CDC73 genes. The disease may be undiagnosed in the absence of a history suggestive of FHPT. Young PHPT patients (≤45 years of age) are more likely to harbor occult FPHPT.

PY - 2012/4/1

Y1 - 2012/4/1

UR - https://link.springer.com/content/pdf/10.1007%2Fs12672-011-0100-8.pdf

U2 - 10.1007/s12672-011-0100-8

DO - 10.1007/s12672-011-0100-8

M3 - Article

VL - 3

JO - Hormones and Cancer

JF - Hormones and Cancer

ER -

Frequent Germ-Line Mutations of the MEN1, CASR, and HRPT2/CDC73 Genes in Young Patients with Clinically Non-familial Primary Hyperparathyroidism

Disciplines

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