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Phenotypic variability of a likely FA2H founder mutation in a family with complicated hereditary spastic paraplegia

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書目詳細資料
發表在:Clin Genet
Main Authors: Donkervoort, Sandra, Dastgir, Jahannaz, Hu, Ying, Zein, Wadih, Marks, Harold, Blackstone, Craig, Bönnemann, Carsten G.
格式: Artigo
語言:Inglês
出版: 2013
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC5030767/
https://ncbi.nlm.nih.gov/pubmed/23745665
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.12185
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