Expression and somatic mutations of SDHAF2 (SDH5), a novel endocrine tumor suppressor gene in parathyroid tumors of primary hyperparathyroidism.

Lee F. Starker; Alberto Delgado-Verdugo; Robert Udelsman; Peyman Björklund; Tobias Carling

doi:10.1007/s12020-010-9399-0

Expression and somatic mutations of SDHAF2 (SDH5), a novel endocrine tumor suppressor gene in parathyroid tumors of primary hyperparathyroidism.

Lee F. Starker, Alberto Delgado-Verdugo, Robert Udelsman, Peyman Björklund, Tobias Carling

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

Original language	American English
Journal	Endocrine
Volume	38
DOIs	https://doi.org/10.1007/s12020-010-9399-0
State	Published - Jan 12 2010
Externally published	Yes

Disciplines

Biology
Genetics
Endocrinology
Medicine and Health Sciences
Internal Medicine
Oncology

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10.1007/s12020-010-9399-0License: Unspecified

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title = "Expression and somatic mutations of SDHAF2 (SDH5), a novel endocrine tumor suppressor gene in parathyroid tumors of primary hyperparathyroidism.",

author = "Starker, \{Lee F.\} and Alberto Delgado-Verdugo and Robert Udelsman and Peyman Bj{\"o}rklund and Tobias Carling",

note = "To investigate the SDHAF2 gene and its effect on primary hyperparathyroidism. Parathyroid tumors causing primary hyperparathyroidism (pHPT) are one of the more common endocrine neoplasias. Loss of heterozygosity at chromosome 11q13 is the most common chromosomal aberration in parathyroid tumors occurring in about 40\% of sporadic tumors.",

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doi = "10.1007/s12020-010-9399-0",

language = "American English",

volume = "38",

journal = "Endocrine",

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T1 - Expression and somatic mutations of SDHAF2 (SDH5), a novel endocrine tumor suppressor gene in parathyroid tumors of primary hyperparathyroidism.

AU - Starker, Lee F.

AU - Delgado-Verdugo, Alberto

AU - Udelsman, Robert

AU - Björklund, Peyman

AU - Carling, Tobias

N1 - To investigate the SDHAF2 gene and its effect on primary hyperparathyroidism. Parathyroid tumors causing primary hyperparathyroidism (pHPT) are one of the more common endocrine neoplasias. Loss of heterozygosity at chromosome 11q13 is the most common chromosomal aberration in parathyroid tumors occurring in about 40% of sporadic tumors.

PY - 2010/1/12

Y1 - 2010/1/12

UR - https://link.springer.com/content/pdf/10.1007%2Fs12020-010-9399-0.pdf

U2 - 10.1007/s12020-010-9399-0

DO - 10.1007/s12020-010-9399-0

M3 - Article

VL - 38

JO - Endocrine

JF - Endocrine

ER -

Expression and somatic mutations of SDHAF2 (SDH5), a novel endocrine tumor suppressor gene in parathyroid tumors of primary hyperparathyroidism.

Disciplines

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