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Medical Dictionary

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Lamin A

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Lamin A Lamin A, abbreviated LMNA, is a gene on chromosome 1 that encodes a protein which is a key component of the membrane surrounding the cell nucleus. Mutations in the LMNA gene are responsible for a number of genetic disorders including: Progeria syndrome, Emery-Dreifuss muscular dystrophy type 2, Limb girdle muscular dystrophy type 1B, Charcot-Marie-Tooth disorder type 2B1, The Dunnigan type of familial partial lipodystrophy, Mandibuloacral dysplasia and A familial form of dilated cardiomyopathy.
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"Lamin A" shown in the following materials:
Researchers from Queen Mary, University of London, have developed a new gene test that detects precancerous cells in patients with mouth lesions. They think that the test could offer the possibility of early and[...]

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