Vocal Cord Paresis and Probable X-Linked Charcot—Marie—Tooth Disease With Novel GJB1 Mutation
Author:
Publisher
Informa UK Limited
Subject
General Medicine,General Neuroscience
Link
http://www.tandfonline.com/doi/pdf/10.3109/00207454.2010.513461
Reference10 articles.
1. Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene
2. X-linked Charcot-Marie-Tooth Disease and Connexin32
3. Novel mutation in X-linked Charcot-Marie-Tooth disease associated with CNS impairment
4. Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene
5. Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations
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3. A Family with Vocal Cord Paralysis Associated with GDAP1 Mutation in Giresun, Turkey;Türk Nöroloi Dergisi;2015-09-05
4. JS-X syndrome: A multiple congenital malformation with vocal cord paralysis, ear deformity, hearing loss, shoulder musculature underdevelopment, and X-linked recessive inheritance;International Journal of Pediatric Otorhinolaryngology;2015-07
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