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

38 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

Vigouroux, C., Caux, F., Capeau, J., Christin-Maitre, S., Cohen, A., Bonne, G., Levy, N., Oshima, J., Garg, A., Martin, G. M., & Kennedy, B. K. (2003). LMNA mutations in atypical Werner's syndrome [5] (multiple letters). Lancet, 362(9395), 1585-1586. https://doi.org/10.1016/S0140-6736(03)14760-5

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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

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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 -