Autosomal dominant hereditary spastic paraplegia: Novel mutations in the <it>REEP1 </it>gene (SPG31)
<p>Abstract</p> <p>Background</p> <p>Mutations in the <it>SPG4 </it>gene (spastin) and in the <it>SPG3A </it>gene (atlastin) account for the majority of 'pure' autosomal dominant form of hereditary spastic paraplegia (HSP). Recently, mu...
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Asıl Yazarlar: | Epplen Joerg T (Yazar), Arning Larissa (Yazar), Schlang Katharina J (Yazar), Stemmler Susanne (Yazar) |
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Materyal Türü: | Kitap |
Baskı/Yayın Bilgisi: |
BMC,
2008-07-01T00:00:00Z.
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