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Novel LMNA mutations seen in patients with...

Journal article

Novel LMNA mutations seen in patients with familial partial lipodystrophy subtype 2 (FPLD2; MIM 151660)

Authors

Lanktree M; Cao H; Rabkin S; Hanna A; Hegele R

Journal

Clinical Genetics, Vol. 71, No. 2, pp. 183–186

Publisher

Wiley

Publication Date

February 2007

DOI

10.1111/j.1399-0004.2007.00740.x

ISSN

0009-9163

Associated Experts

Matthew Lanktree

Associate Professor, Faculty of Health Sciences

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Labels

Fields of Research (FoR)

31 Biological Sciences 32 Biomedical and Clinical Sciences 3202 Clinical sciences 3105 Genetics

Medical Subject Headings (MeSH)

Aged Amino Acid Sequence Base Sequence DNA Female Humans Lamin Type A Lipodystrophy, Familial Partial Male Middle Aged Mutation, Missense Phenotype

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