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A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family.(Report)

Wakil, Salma M. ; Bohlega, Saeed ; Hagos, Samya ; Baz, Batoul ; Dossari, Haya Al ; Ramzan, Khushnooda ; Al - Hassnan, Zuhair N.

European Journal of Medical Genetics, Jan, 2013, Vol.56(1), p.43(3) [Periódico revisado por pares]

Cengage Learning, Inc.

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A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family
Material Type:
Artigo
Adicionar ao Meu Espaço

A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family

Wakil, Salma M. ; Bohlega, Saeed ; Hagos, Samya ; Baz, Batoul ; Al Dossari, Haya ; Ramzan, Khushnooda ; Al-Hassnan, Zuhair N.

European Journal of Medical Genetics, 1/2013, Vol.56(1), pp.43-45 [Periódico revisado por pares]

Elsevier (via CrossRef)

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Artigo
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A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family

Wakil, Salma M ; Bohlega, Saeed ; Hagos, Samya ; Baz, Batoul ; Al Dossari, Haya ; Ramzan, Khushnooda ; Al-Hassnan, Zuhair N

European journal of medical genetics, January 2013, Vol.56(1), pp.43-5 [Periódico revisado por pares]

MEDLINE/PubMed (U.S. National Library of Medicine)

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Material Type:
Artigo
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A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family

Wakil, Salma M ; Bohlega, Saeed ; Hagos, Samya ; Baz, Batoul ; Al Dossari, Haya ; Ramzan, Khushnooda ; Al-Hassnan, Zuhair N

European Journal of Medical Genetics, January 2013, Vol.56(1), pp.43-45 [Periódico revisado por pares]

ScienceDirect Journals (Elsevier)

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