LGMD2L with bone affection: overlapping phenotype of dominant and recessive ANO5-induced disease

7 Citations (Scopus)
Original languageEnglish
JournalMuscle & Nerve
Volume46
Issue number5
Pages (from-to)829-30
Number of pages2
ISSN0148-639X
DOIs
Publication statusPublished - 2012

Keywords

  • Bone Diseases, Developmental
  • Chloride Channels
  • Creatine Kinase
  • Genes, Dominant
  • Genes, Recessive
  • Humans
  • Male
  • Muscular Dystrophies, Limb-Girdle
  • Phenotype
  • Young Adult

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