1.

Premature termination codon mutations in ABCA7 contribute to Alzheimer's disease risk in Belgian patients.

2.

Premature termination codon mutations in ABCA7 contribute to Alzheimer's disease risk in Belgian patients.

3.

Premature termination codon mutations in ABCA7 contribute to Alzheimer's disease risk in Belgian patients.

1.

Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

1.

Reverse genetic screen for loss-of-function mutations uncovers a frame-shifting deletion in the melanophilin gene accountable for a distinctive coat-color in Belgian Blue Cattle.

1.

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.

2.

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.

3.

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.

4.

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.

5.

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.

6.

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.

7.

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.