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Charcot-Marie-Tooth Disease With Episodic Rhabdomyolysis Due to Two Novel Mutations in the β Subunit of Mitochondrial Trifunctional Protein and Effective Response to Modified Diet Therapy.

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Title: Charcot-Marie-Tooth Disease With Episodic Rhabdomyolysis Due to Two Novel Mutations in the β Subunit of Mitochondrial Trifunctional Protein and Effective Response to Modified Diet Therapy.
Authors: Guan Y; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China., Zhang Y; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China., Shen XM; Department of Neurology, Mayo Clinic, Rochester, MN, United States., Zhou L; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China., Shang X; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China., Peng Y; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China., Hu Y; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China., Li W; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Source: Frontiers in neurology [Front Neurol] 2021 Oct 12; Vol. 12, pp. 694966. Date of Electronic Publication: 2021 Oct 12 (Print Publication: 2021).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101546899 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2295 (Print) Linking ISSN: 16642295 NLM ISO Abbreviation: Front Neurol Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Charcot-Marie-Tooth Disease With Episodic Rhabdomyolysis Due to Two Novel Mutations in the β Subunit of Mitochondrial Trifunctional Protein and Effective Response to Modified Diet Therapy.
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  Data: <searchLink fieldCode="AU" term="%22Guan+Y%22">Guan Y</searchLink>; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.<br /><searchLink fieldCode="AU" term="%22Zhang+Y%22">Zhang Y</searchLink>; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.<br /><searchLink fieldCode="AU" term="%22Shen+XM%22">Shen XM</searchLink>; Department of Neurology, Mayo Clinic, Rochester, MN, United States.<br /><searchLink fieldCode="AU" term="%22Zhou+L%22">Zhou L</searchLink>; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.<br /><searchLink fieldCode="AU" term="%22Shang+X%22">Shang X</searchLink>; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.<br /><searchLink fieldCode="AU" term="%22Peng+Y%22">Peng Y</searchLink>; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.<br /><searchLink fieldCode="AU" term="%22Hu+Y%22">Hu Y</searchLink>; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.<br /><searchLink fieldCode="AU" term="%22Li+W%22">Li W</searchLink>; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
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  Data: <searchLink fieldCode="JN" term="%22101546899%22">Frontiers in neurology</searchLink> [Front Neurol] 2021 Oct 12; Vol. 12, pp. 694966. <i>Date of Electronic Publication: </i>2021 Oct 12 (<i>Print Publication: </i>2021).
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              Text: 2021 Oct 12
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