Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia.

Authors:
Chen H; von Hehn C; Kaczmarek LK; Ment LR; Pober BR and 1 more

Journal:
Neurogenetics

Publication Year: 2006

DOI:
10.1007/s10048-006-0071-z

PMCID:
PMC1820748

PMID:
17136396

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Journal Information

Full Title: Neurogenetics

Abbreviation: Neurogenetics

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Neurology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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Evidence found in paper:

"The authors thank the family members for their participation and Dr. Dimitri M. Kullmann (Institute of Neurology, University College of London) for the Kv1.1 clone. FMH was supported by a Paul Beeson Physician Faculty Scholar Award from the American Federation for Aging Research. HC, CvH, and LKK were supported by NIH grant DC01919 to LKK."

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Last Updated: Aug 05, 2025