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Previously Unreported Biallelic Mutation in DNAJC19: Are Sensorineural Hearing Loss and Basal Ganglia Lesions Additional Features of Dilated Cardiomyopathy and Ataxia (DCMA) Syndrome?
Background: Dilated cardiomyopathy (DCM), non-progressive cerebellar ataxia (A), testicular dysgenesis, growth failure, and 3-methylglutaconic aciduria are the hallmarks of DNAJC19 defect (or DCMA syndrome) due to biallelic mutations in DNAJC19. To date DCMA syndrome has been reported in 19 patients...
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Vydáno v: | JIMD Rep |
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Hlavní autoři: | , , , , , |
Médium: | Artigo |
Jazyk: | Inglês |
Vydáno: |
Springer Berlin Heidelberg
2016
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Témata: | |
On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5585102/ https://ncbi.nlm.nih.gov/pubmed/27928778 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2016_23 |
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