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http://dx.doi.org/10.1111/1346-8138.12474 | DOI Listing |
J Dermatol
May 2014
Institute of Dermatology and Department of Dermatology at No. 1 Hospital, Anhui Medical University, Hefei, Anhui, China; State Key Laboratory of Dermatology, Ministry of Science and Technology, Hefei, Anhui, China.
J Child Neurol
April 2010
Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.
Andersen cardiodysrhythmic periodic paralysis or Andersen-Tawil syndrome includes the distinct clinical features of periodic paralysis, cardiac arrhythmia, and facial and skeletal dysmorphisms and exhibits autosomal dominant inheritance. Mutations in the KCNJ2 gene, which encodes the human inward rectifier potassium channel Kir2.1, have been identified in the majority of cases.
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