Hutchinson–Gilford Syndrome (Progeria) with Heterozygous Mutation in the LMNA Gene-ENST00000368300.9 Presenting with Mandibuloacral Dysplasia and Acrogeroid Features—Overlap of Premature Aging Syndromes

Detalles Bibliográficos
Autores principales: Muralidharan, Sniya, Nair, Sukumaran Pradeep, Hariharan, Sankar V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Concise Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9595151/
https://www.ncbi.nlm.nih.gov/pubmed/36304657
http://dx.doi.org/10.4103/idoj.idoj_635_21
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author Muralidharan, Sniya
Nair, Sukumaran Pradeep
Hariharan, Sankar V.
author_facet Muralidharan, Sniya
Nair, Sukumaran Pradeep
Hariharan, Sankar V.
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spelling pubmed-95951512022-10-26 Hutchinson–Gilford Syndrome (Progeria) with Heterozygous Mutation in the LMNA Gene-ENST00000368300.9 Presenting with Mandibuloacral Dysplasia and Acrogeroid Features—Overlap of Premature Aging Syndromes Muralidharan, Sniya Nair, Sukumaran Pradeep Hariharan, Sankar V. Indian Dermatol Online J Concise Communication Wolters Kluwer - Medknow 2022-09-05 /pmc/articles/PMC9595151/ /pubmed/36304657 http://dx.doi.org/10.4103/idoj.idoj_635_21 Text en Copyright: © 2022 Indian Dermatology Online Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Concise Communication
Muralidharan, Sniya
Nair, Sukumaran Pradeep
Hariharan, Sankar V.
Hutchinson–Gilford Syndrome (Progeria) with Heterozygous Mutation in the LMNA Gene-ENST00000368300.9 Presenting with Mandibuloacral Dysplasia and Acrogeroid Features—Overlap of Premature Aging Syndromes
title Hutchinson–Gilford Syndrome (Progeria) with Heterozygous Mutation in the LMNA Gene-ENST00000368300.9 Presenting with Mandibuloacral Dysplasia and Acrogeroid Features—Overlap of Premature Aging Syndromes
title_full Hutchinson–Gilford Syndrome (Progeria) with Heterozygous Mutation in the LMNA Gene-ENST00000368300.9 Presenting with Mandibuloacral Dysplasia and Acrogeroid Features—Overlap of Premature Aging Syndromes
title_fullStr Hutchinson–Gilford Syndrome (Progeria) with Heterozygous Mutation in the LMNA Gene-ENST00000368300.9 Presenting with Mandibuloacral Dysplasia and Acrogeroid Features—Overlap of Premature Aging Syndromes
title_full_unstemmed Hutchinson–Gilford Syndrome (Progeria) with Heterozygous Mutation in the LMNA Gene-ENST00000368300.9 Presenting with Mandibuloacral Dysplasia and Acrogeroid Features—Overlap of Premature Aging Syndromes
title_short Hutchinson–Gilford Syndrome (Progeria) with Heterozygous Mutation in the LMNA Gene-ENST00000368300.9 Presenting with Mandibuloacral Dysplasia and Acrogeroid Features—Overlap of Premature Aging Syndromes
title_sort hutchinson–gilford syndrome (progeria) with heterozygous mutation in the lmna gene-enst00000368300.9 presenting with mandibuloacral dysplasia and acrogeroid features—overlap of premature aging syndromes
topic Concise Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9595151/
https://www.ncbi.nlm.nih.gov/pubmed/36304657
http://dx.doi.org/10.4103/idoj.idoj_635_21
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