LMNA mutations in atypical Werner's syndrome [5] (multiple letters)

C. Vigouroux; F. Caux; J. Capeau; S. Christin-Maitre; A. Cohen; Gisele Bonne; Nicolas Levy; Junko Oshima; Abhimanyu Garg; George M. Martin; Brian K. Kennedy

doi:10.1016/S0140-6736(03)14760-5

LMNA mutations in atypical Werner's syndrome [5] (multiple letters)

C. Vigouroux, F. Caux, J. Capeau, S. Christin-Maitre, A. Cohen, Gisele Bonne, Nicolas Levy, Junko Oshima, Abhimanyu Garg, George M. Martin, Brian K. Kennedy

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

42 Scopus citations

Original language	English (US)
Pages (from-to)	1585-1586
Number of pages	2
Journal	Lancet
Volume	362
Issue number	9395
DOIs	https://doi.org/10.1016/S0140-6736(03)14760-5
State	Published - Nov 8 2003

ASJC Scopus subject areas

Medicine(all)

Access to Document

10.1016/S0140-6736(03)14760-5

Cite this

@article{489ac46557e047d0a5fc9ff5e710104b,

title = "LMNA mutations in atypical Werner's syndrome [5] (multiple letters)",

author = "C. Vigouroux and F. Caux and J. Capeau and S. Christin-Maitre and A. Cohen and Gisele Bonne and Nicolas Levy and Junko Oshima and Abhimanyu Garg and Martin, {George M.} and Kennedy, {Brian K.}",

year = "2003",

month = nov,

day = "8",

doi = "10.1016/S0140-6736(03)14760-5",

language = "English (US)",

volume = "362",

pages = "1585--1586",

journal = "The Lancet",

issn = "0140-6736",

publisher = "Elsevier Limited",

number = "9395",

}

TY - JOUR

T1 - LMNA mutations in atypical Werner's syndrome [5] (multiple letters)

AU - Vigouroux, C.

AU - Caux, F.

AU - Capeau, J.

AU - Christin-Maitre, S.

AU - Cohen, A.

AU - Bonne, Gisele

AU - Levy, Nicolas

AU - Oshima, Junko

AU - Garg, Abhimanyu

AU - Martin, George M.

AU - Kennedy, Brian K.

PY - 2003/11/8

Y1 - 2003/11/8

UR - http://www.scopus.com/inward/record.url?scp=1342284873&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=1342284873&partnerID=8YFLogxK

U2 - 10.1016/S0140-6736(03)14760-5

DO - 10.1016/S0140-6736(03)14760-5

M3 - Letter

C2 - 14615128

AN - SCOPUS:1342284873

VL - 362

SP - 1585

EP - 1586

JO - The Lancet

JF - The Lancet

SN - 0140-6736

IS - 9395

ER -

LMNA mutations in atypical Werner's syndrome [5] (multiple letters)

ASJC Scopus subject areas

Access to Document

Other files and links

Cite this