Dysferlinopathy: Spectrum of pathological changes in skeletal muscle tissue
Background: Dysferlinopathy is an autosomal recessive-limb girdle muscular dystrophy (AR-LGMD) caused due to the defect in gene encoding dysferlin, a sarcolemmal protein. Awareness of the variants and their relative frequency is essential for accurate diagnosis. Aim: To study the spectrum of morphol...
Saved in:
Main Authors: | N Gayathri (Author), R Alefia (Author), A Nalini (Author), T C Yasha (Author), M Anita (Author), Vani Santosh (Author), S K Shankar (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2011-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Water T2 could predict functional decline in patients with dysferlinopathy
by: Ursula Moore, et al.
Published: (2022) -
В6.А-DYSFPRMD/GENEJ MICE AS A GENETIC MODEL OF DYSFERLINOPATHY
by: M. V. Korokin, et al.
Published: (2022) -
Three‐year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy
by: Harmen Reyngoudt, et al.
Published: (2022) -
Identification of Novel Antisense-Mediated Exon Skipping Targets in DYSF for Therapeutic Treatment of Dysferlinopathy
by: Joshua J.A. Lee, et al.
Published: (2018) -
Tissue Engineered Strategies for Skeletal Muscle Injury
by: Umile Giuseppe Longo, et al.
Published: (2012)