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011 Des mutations inactivatrices de la périlipine sont responsables d’un syndrome lipodystrophique de transmission autosomique dominante chez l’homme by C. Le Dour; S. Gandotra; W. Bottomley; P. Cervera; P. Giral; Y. Reznik; G. Charpentier; M. Auclair; M. Auclair; O. Lascols; J. Capeau; S. O’Rahilly; D. Savage; C. Vigouroux is a Medicine article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Medicine.

Author
C. Le Dour; S. Gandotra; W. Bottomley; P. Cervera; P. Giral; Y. Reznik; G. Charpentier; M. Auclair; M. Auclair; O. Lascols; J. Capeau; S. O’Rahilly; D. Savage; C. Vigouroux
Publisher
Masson Editeur; Elsevier ; Elsevier Masson; Elsevier BV (ISSN 1262-3636)
Published
2011
Language
FR
Field
Medicine (Health Sciences)

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