Dunnigan-type familial partial lipodystrophy associated with the heterozygous R482W mutation in LMNA gene — case study of three women from one family-Reference-Cited by-同舟云学术

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Dunnigan-type familial partial lipodystrophy associated with the heterozygous R482W mutation in LMNA gene — case study of three women from one family

Published:2013-09-04 Issue:4 Volume:64 Page:306-311
ISSN:0423-104X
Container-title:Endokrynologia Polska
language:
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Author:

Nabrdalik Katarzyna,Strózik Agnieszka,Minkina-Pędras Mariola,Jarosz-Chobot Przemysława,Młynarski Wojciech,Grzeszczak Władysław,Gumprecht Janusz

Publisher

VM Media SP. zo.o VM Group SK

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. High-throughput Second-generation Sequencing Technology Assisted Diagnosis of Familial Partial Lipodystrophy (Type 2 Kobberling-Dunnigan Syndrome): A Case Report;Combinatorial Chemistry & High Throughput Screening;2024-02

2. Deciphering the Clinical Presentations in LMNA-related Lipodystrophy: Report of 115 Cases and a Systematic Review;The Journal of Clinical Endocrinology & Metabolism;2023-10-16

3. Clinical Spectrum of LMNA-Associated Type 2 Familial Partial Lipodystrophy: A Systematic Review;Cells;2023-02-24

4. The LEM-ESCRT toolkit: Repair and maintenance of the nucleus;Frontiers in Cell and Developmental Biology;2022-09-12

5. Genetic syndromes with diabetes: A systematic review;Obesity Reviews;2021-07-15

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