Open AccessHutchinson–Gilford syndrome (Progeria) with heterozygous mutation in the LMNA Gene-ENST00000368300.9 presenting with mandibuloacral dysplasia and acrogeroid features—overlap of premature aging syndromes
Author(s) -
Sniya Muralidharan,
Sukumaran Pradeep Nair,
Sankar V Hariharan
Publication year - 2022
Publication title -
indian dermatology online journal
Language(s) - English
Resource type - Journals
eISSN - 2249-5673
pISSN - 2229-5178
DOI - 10.4103/idoj.idoj_635_21
Subject(s) - lmna , progeria , premature aging , medicine , lamin , gene mutation , genetics , mutation , pathology , biology , gene , physiology
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom