• 'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband Syndromes
• "Electrifying dysmorphology": Potassium channelopathies causing dysmorphic syndromes
• Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants
• Clinical and genetic evaluations of Zimmermann-Laband syndrome with gingival fibromatosis: a rare case report
• Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature review
• Epilepsy in KCNH1-related syndromes
• Establishment and characterization of ZJUCHi003: an induced pluripotent stem cell line from a patient with Temple-Baraitser/Zimmermann-Laband syndrome carrying KCNH1 c.1070G > A (p.R357Q) variant
• Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca²⁺-Activated K⁺ Channel SK3 Cause Zimmermann-Laband Syndrome
• Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes
• Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome
• Patients with <em>KCNH1</em>-related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome
• Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis
• Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K⁺ channelopathies
• Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome: one clinical entity?
• The orthodontic and surgical management of Zimmerman-Laband syndrome
• Zimmermann-Laband syndrome and infantile systemic hyalinosis: an enigma with two separate terms with overlapping features: a case report
• Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant
• Zimmermann-Laband syndrome: a case report