Fibulin-5 mutation featuring Charcot-Marie-Tooth disease, joint hyperlaxity, and scoliosis

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Bibliographic Details
Published in:	Neurol Genet
Main Authors:	Kazamel, Mohamed, Lopez, Michael A., Bebin, Martina, Bowling, Kevin, Korf, Bruce R., Barsh, Gregory S., Cooper, Gregory M., Hurst, Anna C.E., Ubogu, Eroboghene E.
Format:	Artigo
Language:	Inglês
Published:	Wolters Kluwer 2020
Subjects:	Clinical/Scientific Notes
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC7413605/ https://ncbi.nlm.nih.gov/pubmed/32802946 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000476
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