Myogenes and Myotubes

S. T. Iannaccone

doi:10.1177/088307389200700208

Myogenes and Myotubes

S. T. Iannaccone

Research output: Contribution to journal › Article › peer-review

2 Scopus citations

Abstract

Investigation of the congenital myopathies has been limited by a lack of knowledge regarding basic mechanisms involved in normal myogenesis of human muscle and the relative rarity of these diseases. A newly recognized family of regulatory genes has been shown to be necessary for myogenesis to proceed to formation of normal mature muscle. It is likely that investigation of patients with one or more types of structural myopathy may show that abnormalities of the regulatory basic helix-loop-helix (bHLH) genes may be responsible for disease. (J Child Neurol 1992;7:180-187).

Original language	English (US)
Pages (from-to)	180-187
Number of pages	8
Journal	Journal of child neurology
Volume	7
Issue number	2
DOIs	https://doi.org/10.1177/088307389200700208
State	Published - Apr 1992

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Clinical Neurology

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title = "Myogenes and Myotubes",

abstract = "Investigation of the congenital myopathies has been limited by a lack of knowledge regarding basic mechanisms involved in normal myogenesis of human muscle and the relative rarity of these diseases. A newly recognized family of regulatory genes has been shown to be necessary for myogenesis to proceed to formation of normal mature muscle. It is likely that investigation of patients with one or more types of structural myopathy may show that abnormalities of the regulatory basic helix-loop-helix (bHLH) genes may be responsible for disease. (J Child Neurol 1992;7:180-187).",

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AB - Investigation of the congenital myopathies has been limited by a lack of knowledge regarding basic mechanisms involved in normal myogenesis of human muscle and the relative rarity of these diseases. A newly recognized family of regulatory genes has been shown to be necessary for myogenesis to proceed to formation of normal mature muscle. It is likely that investigation of patients with one or more types of structural myopathy may show that abnormalities of the regulatory basic helix-loop-helix (bHLH) genes may be responsible for disease. (J Child Neurol 1992;7:180-187).

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Myogenes and Myotubes

Abstract

ASJC Scopus subject areas

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