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Diseases caused by mutations in LMNB1 and LMNB2 encoding B-type lamins. On-line Mendelian Inheritance in Man entry numbers are given in parentheses.
| LMNB1 |
| Adult-onset, Autosomal dominant Leukodystrophy (#169500) |
| LMNB2 |
| Barraquer-Simons Syndrome, Heterozygous Mutations (#608709) |
