Literature DB >> 31742230

Erratum: Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy.

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Abstract

[This corrects the article on p. e305 in vol. 5, PMID: 30842973.].
© 2019 American Academy of Neurology.

Entities:  

Year:  2019        PMID： 31742230      PMCID： PMC6807656          DOI： 10.1212/NXG.0000000000000362

Source DB:  PubMed          Journal:  Neurol Genet        ISSN： 2376-7839


  1 in total

1.  Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy.

Authors:  Bruce Nmezi; Elisa Giorgio; Raili Raininko; Anna Lehman; Malte Spielmann; Mary Kay Koenig; Rahmat Adejumo; Melissa Knight; Ralitza Gavrilova; Murad Alturkustani; Manas Sharma; Robert Hammond; William A Gahl; Camilo Toro; Alfredo Brusco; Quasar S Padiath
Journal:  Neurol Genet       Date:  2019-01-24
  1 in total

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