Fibulin-5 mutation featuring Charcot-Marie-Tooth disease, joint hyperlaxity, and scoliosis.
Mohamed KazamelMichael A LopezMartina BebinKevin BowlingBruce R KorfGregory S BarshGregory M CooperAnna C E HurstEroboghene E UboguPublished in: Neurology. Genetics (2020)
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