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Hereditary Transthyretin Amyloidosis in Eight Chinese Families

BACKGROUND: Mutations of transthyretin (TTR) cause the most common type of autosomal-dominant hereditary systemic amyloidosis, which occurs worldwide. To date, more and more mutations in the TTR gene have been reported. Some variations in the clinical presentation are often observed in patients with...

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Bibliografische gegevens
Gepubliceerd in:Chin Med J (Engl)
Hoofdauteurs: Meng, Ling-Chao, Lyu, He, Zhang, Wei, Liu, Jing, Wang, Zhao-Xia, Yuan, Yun
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Medknow Publications & Media Pvt Ltd 2015
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4756886/
https://ncbi.nlm.nih.gov/pubmed/26521788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0366-6999.168048
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