Henny H. Lemmink
University Medical Center Groningen(NL)University Medical Center Groningen(NL)University of Groningen(NL)Amyloidosis Foundation(US)
Publications by Year
Research Areas
Skin and Cellular Biology Research, RNA modifications and cancer, Neurogenetic and Muscular Disorders Research, Cell Adhesion Molecules Research, Autoimmune Bullous Skin Diseases
Most-Cited Works
- → Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome(1994)511 cited
- → Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome(2000)288 cited
- → Muscle strength and motor function throughout life in a cross‐sectional cohort of 180 patients with spinal muscular atrophy types 1c–4(2017)225 cited
- → Mutations in the type IV collagen α3 (COL4A3) gene in autosomal recessive Alport syndrome(1994)215 cited
- → Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.(1996)202 cited
- → Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650](1997)190 cited