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NG1872
NG1872
http://dx.doi.org/10.1038/NG1872
Lamin B1 duplications cause autosomal dominant leukodystrophy
P356
Q28261772-EFEED914-46FC-4291-898C-BFFBB000C4FA
P356
NG1872
http://dx.doi.org/10.1038/NG1872