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Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation.
Clinical Genetics ( IF 2.9 ) Pub Date : 2020-07-28 , DOI: 10.1111/cge.13809 Marta Lamartine S Monteiro 1 , Isabelle Vandernoot 2 , Laurence Desmyter 2 , Vanessa Wermenbol 3 , Gilles Naeije 4 , Gauthier Remiche 1
Clinical Genetics ( IF 2.9 ) Pub Date : 2020-07-28 , DOI: 10.1111/cge.13809 Marta Lamartine S Monteiro 1 , Isabelle Vandernoot 2 , Laurence Desmyter 2 , Vanessa Wermenbol 3 , Gilles Naeije 4 , Gauthier Remiche 1
Affiliation
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Siblings with hereditary spastic paraplegia and corpus callosum thinning associated with a novel TUBβ4A mutation.
中文翻译：
常染色体显性遗传性痉挛性截瘫伴有新的TUBβ4A突变的call体变薄。
具有遗传性痉挛性截瘫和call体变薄的兄弟姐妹与新的TUBβ4A突变相关。
更新日期：2020-09-23
中文翻译：
常染色体显性遗传性痉挛性截瘫伴有新的TUBβ4A突变的call体变薄。
具有遗传性痉挛性截瘫和call体变薄的兄弟姐妹与新的TUBβ4A突变相关。
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