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Developmental Biology, ISSN 0012-1606, 12/2018, Volume 444, Issue Suppl 1, pp. S297 - S307
Mutations that disrupt the inwardly rectifying potassium channel Kir2.1 lead to Andersen-Tawil syndrome that includes periodic paralysis, cardiac arrhythmia,... 
SENSITIVE POTASSIUM CHANNELS | KCNJ11 ACTIVATING MUTATIONS | OSTEOBLAST DIFFERENTIATION | DOPAMINE RELEASE | ZIMMERMANN-LABAND SYNDROME | RECEPTOR | RECTIFYING K+ CHANNEL | DEVELOPMENTAL BIOLOGY | EXPRESSION | KEPPEN-LUBINSKY SYNDROME | TEMPLE-BARAITSER | Heart | Medical colleges
Journal Article
Epileptic disorders, ISSN 1294-9361, 06/2016, Volume 18, Issue 2, pp. 123 - 136
Aim. KCNH1 mutations have been identified in patients with Zimmermann-Laband syndrome and Temple-Baraitser syndrome, as well as patients with uncharacterized... 
KCNH1-related encephalopathy | undefined intellectual disability | Zimmermann-Laband syndrome | genetic epilepsy | MICE | Temple-Baraitser syndrome | MUTATIONS | Temple‐Baraitser syndrome | KCNH1‐related encephalopathy | Zimmermann‐Laband syndrome | KCNH1-Related encephalopathy | Zimmermann-laband syndrome | Temple-baraitser syndrome | Genetic epilepsy | Undefined intellectual disability | CLINICAL NEUROLOGY | Hallux - abnormalities | Humans | Thumb - physiopathology | Child, Preschool | Fibromatosis, Gingival - genetics | Infant | Male | Abnormalities, Multiple - drug therapy | Electroencephalography | Craniofacial Abnormalities - physiopathology | Epilepsy - physiopathology | Fibromatosis, Gingival - drug therapy | Nails, Malformed - physiopathology | Intellectual Disability - genetics | Young Adult | Adult | Epilepsy - genetics | Female | Child | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Brain - physiopathology | Anticonvulsants - therapeutic use | Craniofacial Abnormalities - drug therapy | Nails, Malformed - drug therapy | Ether-A-Go-Go Potassium Channels - genetics | Abnormalities, Multiple - physiopathology | Syndrome | Nails, Malformed - genetics | Hand Deformities, Congenital - drug therapy | Intellectual Disability - drug therapy | Intellectual Disability - physiopathology | Fibromatosis, Gingival - physiopathology | Hand Deformities, Congenital - genetics | Hand Deformities, Congenital - physiopathology | Adolescent | Epilepsy - drug therapy | Hallux - physiopathology | Thumb - abnormalities | Convulsions & seizures | Mutation | Intellectual disabilities | Epilepsy
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 10/2016, Volume 170, Issue 10, pp. 2611 - 2616
Journal Article
BIOMEDICINES, ISSN 2227-9059, 09/2019, Volume 7, Issue 3, p. 48
Background: Zimmermann-Laband-1 syndrome (ZLS-1; OMIM# 135500) is a rare genetic disorder whose oral pathognomonic sign is the development of progressive,... 
MEDICINE, RESEARCH & EXPERIMENTAL | oral microbiome | Zimmermann-Laband syndrome | PHARMACOLOGY & PHARMACY | gingival fibromatosis | periodontal disease
Journal Article
Annals of maxillofacial surgery, ISSN 2231-0746, 07/2018, Volume 8, Issue 2, pp. 352 - 354
Zimmermann-Laband syndrome is a rare condition which manifests as hereditary gingival tissue hypertrophy along with other clinical features. Till date, only... 
Usage | Genetic disorders | Research | Gene expression | Oral surgery | twins | Zimmermann–Laband syndrome | Sisters | Case Report - Surgery
Journal Article
Journal Article
Clinical Case Reports, ISSN 2050-0904, 04/2017, Volume 5, Issue 4, pp. 376 - 379
Key Clinical Message Our report clarifies the role of ATP6V1B2 in patients with deafness and onycho‐osteodystrophy and confirms that a recurring ATP6V1B2... 
ATP6V1B2 | dominant deafness–onychodystrophy | Zimmermann–Laband syndrome | deafness–onychodystrophy–osteodystrophy–mental retardation–seizures | whole‐exome sequencing
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 06/2016, Volume 17, Issue 1, p. 42
Journal Article
International Journal of Collaborative Research on Internal Medicine and Public Health, ISSN 1840-4529, 04/2012, Volume 4, Issue 4, pp. 240 - 245
Journal Article