Erratum: Molecular Characterization and Cancer Risk Associated with BRCA1 and BRCA2 Splice Site Variants Identified in Multiple-Case Breast Cancer Families

A. A. Tesoriero; E. M. Wong; Mark A. Jenkins; J. L. Hopper; M. A. Brown; G. Chenevix-Trench; A. B. Spurdle; M. C. Southey

doi:10.1002/humu.22526

Erratum: Molecular Characterization and Cancer Risk Associated with BRCA1 and BRCA2 Splice Site Variants Identified in Multiple-Case Breast Cancer Families

A. A. Tesoriero, E. M. Wong, Mark A. Jenkins, J. L. Hopper, M. A. Brown, G. Chenevix-Trench, A. B. Spurdle, M. C. Southey

Medicine Monash Health

Research output: Contribution to journal › Comment / Debate › Other › peer-review

Original language	English
Pages (from-to)	511
Number of pages	1
Journal	Human Mutation
Volume	35
Issue number	4
DOIs	https://doi.org/10.1002/humu.22526
Publication status	Published - 1 Jan 2014

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10.1002/humu.22526

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title = "Erratum: Molecular Characterization and Cancer Risk Associated with BRCA1 and BRCA2 Splice Site Variants Identified in Multiple-Case Breast Cancer Families",

author = "Tesoriero, {A. A.} and Wong, {E. M.} and Jenkins, {Mark A.} and Hopper, {J. L.} and Brown, {M. A.} and G. Chenevix-Trench and Spurdle, {A. B.} and Southey, {M. C.}",

year = "2014",

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pages = "511",

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T2 - Molecular Characterization and Cancer Risk Associated with BRCA1 and BRCA2 Splice Site Variants Identified in Multiple-Case Breast Cancer Families

AU - Tesoriero, A. A.

AU - Wong, E. M.

AU - Jenkins, Mark A.

AU - Hopper, J. L.

AU - Brown, M. A.

AU - Chenevix-Trench, G.

AU - Spurdle, A. B.

AU - Southey, M. C.

PY - 2014/1/1

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U2 - 10.1002/humu.22526

DO - 10.1002/humu.22526

M3 - Comment / Debate

AN - SCOPUS:84896122881

SN - 1059-7794

VL - 35

SP - 511

JO - Human Mutation

JF - Human Mutation

IS - 4

ER -

Erratum: Molecular Characterization and Cancer Risk Associated with BRCA1 and BRCA2 Splice Site Variants Identified in Multiple-Case Breast Cancer Families

UN SDGs

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Molecular characterization and cancer risk associated with BRCA1 and BRCA2 splice site variants identified in multiple-case breast cancer families

Cite this