Novel LMNA mutations seen in patients with familial partial lipodystrophy subtype 2 (FPLD2; MIM 151660)
Journal Articles
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Overview
status
publication date
- February 2007
has subject area
- 0604 Genetics (FoR)
- 1103 Clinical Sciences (FoR)
- Aged (MeSH)
- Amino Acid Sequence (MeSH)
- Base Sequence (MeSH)
- DNA (MeSH)
- Female (MeSH)
- Genetics & Heredity (Science Metrix)
- Humans (MeSH)
- Lamin Type A (MeSH)
- Lipodystrophy, Familial Partial (MeSH)
- Male (MeSH)
- Middle Aged (MeSH)
- Mutation, Missense (MeSH)
- Phenotype (MeSH)
published in
- Clinical Genetics Journal