Spectrum of Nondystrophic Skeletal Muscle Channelopathies in Children

The nondystrophic skeletal muscle channelopathies are a group of disorders caused by mutations of various voltage-gated ion channel genes, including nondystrophic myotonia and periodic paralysis.

Gespeichert in:
Autor*in:

Al-Ghamdi, Fouad [verfasserIn]

Darras, Basil T.

Ghosh, Partha S.

Format:

E-Artikel

Sprache:

Englisch

Erschienen:

2017

Schlagwörter:

periodic paralysis

skeletal muscle channelopathies

children

nondystrophic myotonia

muscle disorders

Umfang:

8

Übergeordnetes Werk:

Enthalten in: NOVEL INSIGHTS INTO THE PHYSIOLOGY OF CARDIAC-CORONARY INTERACTION: A FIRST-IN-HUMAN STUDY UTILISING INVASIVE REAL-TIME SIMULTANEOUS MEASURES OF CORONARY AND LEFT VENTRICULAR HEMODYNAMICS - Patterson, Tiffany ELSEVIER, 2016, Amsterdam [u.a.]

Übergeordnetes Werk:

volume:70 ; year:2017 ; pages:26-33 ; extent:8

Links:

Volltext

DOI / URN:

10.1016/j.pediatrneurol.2017.02.006

Katalog-ID:

ELV03058132X

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