Sarcolemmal excitability in the myotonic dystrophies-Reference-Cited by-同舟云学术

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Sarcolemmal excitability in the myotonic dystrophies

Published:2017-09-30 Issue:4 Volume:57 Page:595-602
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Boland‐Freitas Robert¹²,Lee James¹,Howells James³,Liang Christina¹,Corbett Alastair⁴,Nicholson Garth⁵,Ng Karl¹³

Affiliation:

1. Department of Neurology and NeurophysiologyRoyal North Shore HospitalReserve RoadSt Leonards New South Wales Australia

2. Department of NeurologyBlacktown HospitalBlacktown New South Wales Australia

3. Sydney Medical SchoolCamperdown New South Wales Australia

4. Department of NeurologyConcord HospitalConcord New South Wales Australia

5. Department of Molecular MedicineConcord HospitalConcord New South Wales Australia

Funder

Allergan and Ipsen Pharmaceuticals

Royal North Shore Hospital Corner Shop

Publisher

Wiley

Subject

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.25962

Reference37 articles.

1. Myotonic Dystrophy

2. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

3. Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9

4. Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms

5. A Muscleblind Knockout Model for Myotonic Dystrophy

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