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Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy
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*
*Corresponding author for this work
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(Scopus)