• <em>STAC3</em> Disorder
• A Neuromuscular Perspective: Why Craniofacial Surgeons/Researchers Need to be Aware of Native American Myopathy?
• Bailey-Bloch Congenital Myopathy in Brazilian Patients: A Very Rare Myopathy with Malignant Hyperthermia Susceptibility
• Challenges in Obstetric Anesthesia in a Parturient With Native American Myopathy: A Case Report
• Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet
• Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3
• Discovery of a Novel Class of Benzimidazole-Based Nicotinic Acetylcholine Receptor Modulators: Positive and Negative Modulation Arising from Overlapping Allosteric Sites
• Duchenne and Becker Muscular Dystrophies' Prevalence in MD STARnet Surveillance Sites: An Examination of Racial and Ethnic Differences
• Effects of AFQ056 on language learning in fragile X syndrome
• Examining the impact of Native American myopathy on the quality of life and healthcare accessibility of patients and caregivers
• Heterogeneous Ni-MoN nanosheet-assembled microspheres for urea-assisted hydrogen production
• Identification of STAC3 variants in non-Native American families with overlapping features of Carey-Fineman-Ziter syndrome and Moebius syndrome
• Increased risk of statin-associated autoimmune myopathy among American Indians
• Is Fibromyalgia Associated with Borrelia-specific T Lymphocytes?
• Malignant Hyperthermia
• Multiple Sequence Variants in STAC3 Affect Interactions with Ca_V1.1 and Excitation-Contraction Coupling
• Muscular strength, mobility in daily life and mental wellbeing among older adult Inuit in Greenland. The Greenland population health survey 2018
• Novel STAC3 Mutations in the First Non-Amerindian Patient with Native American Myopathy
• Post-acute neurological consequences of COVID-19: an unequal burden
• Potential implications of six American Indian patients with myopathy, statin exposure and anti-HMGCR antibodies
• Prevalence of opioid and nonopioid pain management therapies among Medicare beneficiaries with musculoskeletal pain conditions from 2016 to 2019
• Prevalence of protective haplotypes of the <em>SLCO1B1</em> gene for statin transport in Mexican populations
• Skeletal muscle Ca_V1.1 channelopathies
• STAC3 disorder: a common cause of congenital hypotonia in Southern African patients
• STAC3 related congenital myopathy: A case series of seven Comorian patients
• STAC3 stably interacts through its C1 domain with Ca_V1.1 in skeletal muscle triads
• STAC3-related myopathy: A Report of a Cohort of Seven Saudi Arabian Patients
• Statin-associated immune-mediated necrotizing myositis in Native Americans
• Structural insights into binding of STAC proteins to voltage-gated calcium channels
• The First Russian Patient with Native American Myopathy
• When all roads lead to Africa…
• Why Craniofacial Surgeons/Researchers Need to be Aware of Native American Myopathy?