Identification of de novo germline mutations in the HRPT2 gene in two apparently sporadic cases with challenging parathyroid tumor diagnoses.

BM Cavaco; R Santos; A Félix; D Carvalho; JM Lopes; R Domingues; M Sirgado; N Rei; F Fonseca; JR Santos; L Sobrinho; V Leite

doi:10.1007/s12022-011-9151-1

Identification of de novo germline mutations in the HRPT2 gene in two apparently sporadic cases with challenging parathyroid tumor diagnoses.

BM Cavaco, R Santos, A Félix, D Carvalho, JM Lopes, R Domingues, M Sirgado, N Rei, F Fonseca, JR Santos, L Sobrinho, V Leite

Center for Interdisciplinary Research in Health (CIIS)

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

Original language	English
Journal	Endocrine Pathology
DOIs	https://doi.org/10.1007/s12022-011-9151-1
Publication status	Published - Mar 2011

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10.1007/s12022-011-9151-1

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@article{d8289e13a6fd453f8da896f95649f225,

title = "Identification of de novo germline mutations in the HRPT2 gene in two apparently sporadic cases with challenging parathyroid tumor diagnoses.",

author = "BM Cavaco and R Santos and A F{\'e}lix and D Carvalho and JM Lopes and R Domingues and M Sirgado and N Rei and F Fonseca and JR Santos and L Sobrinho and V Leite",

year = "2011",

month = mar,

doi = "10.1007/s12022-011-9151-1",

language = "English",

journal = "Endocrine Pathology",

issn = "1046-3976",

publisher = "Springer",

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TY - JOUR

T1 - Identification of de novo germline mutations in the HRPT2 gene in two apparently sporadic cases with challenging parathyroid tumor diagnoses.

AU - Cavaco, BM

AU - Santos, R

AU - Félix, A

AU - Carvalho, D

AU - Lopes, JM

AU - Domingues, R

AU - Sirgado, M

AU - Rei, N

AU - Fonseca, F

AU - Santos, JR

AU - Sobrinho, L

AU - Leite, V

PY - 2011/3

Y1 - 2011/3

UR - http://europepmc.org/abstract/med/21360064

U2 - 10.1007/s12022-011-9151-1

DO - 10.1007/s12022-011-9151-1

M3 - Article

C2 - 21360064

SN - 1046-3976

JO - Endocrine Pathology

JF - Endocrine Pathology

ER -

Identification of de novo germline mutations in the HRPT2 gene in two apparently sporadic cases with challenging parathyroid tumor diagnoses.

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