Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1(Burin)) in four kindreds from Newfoundland

Shodimu Emmanuel Olufemi; Jane S. Green; Pachiappan Manickam; Siradanahalli C. Guru; Sunita K. Agarwal; Mary Beth Kester; Qihan Dong; A. Lee Burns; Allen M. Spiegel; Stephen J. Marx; Francis S. Collins; Settara C. Chandrasekharappa

doi:10.1002/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V

Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1(Burin)) in four kindreds from Newfoundland

Shodimu Emmanuel Olufemi
, Jane S. Green
, Pachiappan Manickam
, Siradanahalli C. Guru
, Sunita K. Agarwal
, Mary Beth Kester
, Qihan Dong
, A. Lee Burns
, Allen M. Spiegel
, Stephen J. Marx
, Francis S. Collins
, Settara C. Chandrasekharappa

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

Original language	English
Pages (from-to)	264-269
Number of pages	6
Journal	Human Mutation
Volume	11
Issue number	4
DOIs	https://doi.org/10.1002/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V
State	Published - 1998
Externally published	Yes

ASJC Scopus Subject Areas

Genetics
Genetics(clinical)

Keywords

Founder effect
MEN1 gene
MEN1(Burin)
Menin
Newfoundland
Prolactinoma

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10.1002/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V

Cite this

Olufemi, S. E., Green, J. S., Manickam, P., Guru, S. C., Agarwal, S. K., Kester, M. B., Dong, Q., Burns, A. L., Spiegel, A. M., Marx, S. J., Collins, F. S., & Chandrasekharappa, S. C. (1998). Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1(Burin)) in four kindreds from Newfoundland. Human Mutation, 11(4), 264-269. https://doi.org/10.1002/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V

Olufemi, SE, Green, JS, Manickam, P, Guru, SC, Agarwal, SK, Kester, MB, Dong, Q, Burns, AL, Spiegel, AM, Marx, SJ, Collins, FS & Chandrasekharappa, SC 1998, 'Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1(Burin)) in four kindreds from Newfoundland', Human Mutation, vol. 11, no. 4, pp. 264-269. https://doi.org/10.1002/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V

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title = "Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1(Burin)) in four kindreds from Newfoundland",

keywords = "Founder effect, MEN1 gene, MEN1(Burin), Menin, Newfoundland, Prolactinoma",

author = "Olufemi, \{Shodimu Emmanuel\} and Green, \{Jane S.\} and Pachiappan Manickam and Guru, \{Siradanahalli C.\} and Agarwal, \{Sunita K.\} and Kester, \{Mary Beth\} and Qihan Dong and Burns, \{A. Lee\} and Spiegel, \{Allen M.\} and Marx, \{Stephen J.\} and Collins, \{Francis S.\} and Chandrasekharappa, \{Settara C.\}",

year = "1998",

doi = "10.1002/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V",

language = "English",

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T1 - Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1(Burin)) in four kindreds from Newfoundland

AU - Olufemi, Shodimu Emmanuel

AU - Green, Jane S.

AU - Manickam, Pachiappan

AU - Guru, Siradanahalli C.

AU - Agarwal, Sunita K.

AU - Kester, Mary Beth

AU - Dong, Qihan

AU - Burns, A. Lee

AU - Spiegel, Allen M.

AU - Marx, Stephen J.

AU - Collins, Francis S.

AU - Chandrasekharappa, Settara C.

PY - 1998

Y1 - 1998

KW - Founder effect

KW - MEN1 gene

KW - MEN1(Burin)

KW - Menin

KW - Newfoundland

KW - Prolactinoma

UR - https://www.scopus.com/pages/publications/7144229389

UR - https://www.scopus.com/pages/publications/7144229389#tab=citedBy

U2 - 10.1002/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V

DO - 10.1002/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V

M3 - Article

C2 - 9554741

AN - SCOPUS:7144229389

SN - 1059-7794

VL - 11

SP - 264

EP - 269

JO - Human Mutation

JF - Human Mutation

IS - 4

ER -

Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1(Burin)) in four kindreds from Newfoundland

ASJC Scopus Subject Areas

Keywords

Access to Document

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