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Genotype-phenotype association in patients with SCN4A mutation.

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Author(s): El-Battrawy, Ibrahim; Borggrefe, Martin; Lang, Siegried; Zhou, Xiaobo; Akin, Ibrahim
Source:
Lancet. 6/8/2019, Vol. 393 Issue 10188, p2301-2301. 1p.

Additional Information
- Subject Terms:
  PATIENTS; GENETIC techniques; GENETIC mutation; SODIUM; SUDDEN infant death syndrome; CASE-control method; SKELETAL muscle; MEMBRANE transport proteins

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