Associated Papers
KLK15 alters connective tissues in hypermobile Ehlers-Danlos syndrome.
Gensemer C et al.
Iscience, 2025
40949095 (PubMed )
Supplement: mmc1.pdf
Germline variants in early and late-onset Brazilian prostate cancer patients.
Coelho KBCA et al.
Urologic Oncology, 2024
Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes.
Machnicki MM et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2021
33170376 (PubMed )
Supplement: 10072_2020_4876_MOESM3_ESM.xlsx › variants
Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor.
Loules G et al.
Journal of Clinical Medicine, 2020
Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.
Schrader A et al.
Nature Communications, 2018
29449575 (PubMed )
Supplement: 41467_2017_2688_MOESM20_ESM.xlsx › a__Freq_TP094
Sequence variation at KLK and WFDC clusters and its association to semen hyperviscosity and other male infertility phenotypes.
Marques PI et al.
Human Reproduction (oxford, England), 2016
A comprehensive resequence analysis of the KLK15-KLK3-KLK2 locus on chromosome 19q13.33.
Parikh H et al.
Human Genetics, 2010
19823874 (PubMed )
Supplement: 439_2009_751_MOESM5_ESM.pdf
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