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About this Biochemistry, Genetics and Molecular Biology article

First description of a patient with Vici syndrome due to a mutation affecting the penultimate exon of EPG5 and review of the literature by Ehmke, Nadja; Parvaneh, Nima; Krawitz, Peter; Ashrafi, Mahmoud-Reza; Karimi, Parviz; Mehdizadeh, Mehrzad; Krüger, Ulrike; Hecht, Jochen; Mundlos, Stefan; Robinson, Peter N. is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Ehmke, Nadja; Parvaneh, Nima; Krawitz, Peter; Ashrafi, Mahmoud-Reza; Karimi, Parviz; Mehdizadeh, Mehrzad; Krüger, Ulrike; Hecht, Jochen; Mundlos, Stefan; Robinson, Peter N.
Publisher
John Wiley and Sons; Wiley (John Wiley & Sons); Wiley-Liss Inc; Wiley (ISSN 1552-4825)
Published
2014
Language
EN
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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