Plectin defects in epidermolysis bullosa simplex with muscular dystrophy-Reference-Cited by-同舟云学术

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Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Published:2006 Issue:1 Volume:35 Page:24-35
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

McMillan J.R.,Akiyama M.,Rouan F.,Mellerio J.E.,Lane E.B.,Leigh I.M.,Owaribe K.,Wiche G.,Fujii N.,Uitto J.,Eady R.A.J.,Shimizu H.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference52 articles.

1. Possible Role of Cytoskeleton in Intracellular Arrangement and Regulation of Mitochondria

2. . Theory and practice of histological techniques, Vol. 1. London: Churchill Livingstone; 1996. p 343–364.

3. Myopathy, Myasthenic Syndrome, and Epidermolysis Bullosa Simplex Due to Plectin Deficiency

4. Differences in the distribution of synemin, paranemin, and plectin in skeletal muscles of wild-type and desmin knock-out mice

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1. Supraglottic laryngeal manifestation of epidermolysis bullosa in a pediatric population: A literature review with four case reports;Otolaryngology Case Reports;2023-06

2. Epidermolysis Bullosa Simplex with Muscular Dystrophy;Genetic Syndromes;2023

3. Mutation update: The spectra of PLEC sequence variants and related plectinopathies;Human Mutation;2022-07-29

4. Plectin in Skin Fragility Disorders;Cells;2021-10-14

5. Muscle-Related Plectinopathies;Cells;2021-09-19

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