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Your search keyword '"De Jonghe, Peter"' showing total 17 results

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2. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

3. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

4. Dominant NARS1 mutations causing axonal Charcot–Marie–Tooth disease expand NARS1-associated diseases

5. Myelin protein zero mutation‐related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohort

6. Vitamin D3 deficiency and osteopenia in spastic paraplegia type 5 indicate impaired bone homeostasis.

7. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

8. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

9. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

10. Myelin protein zero mutation‐related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohort.

11. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

12. De Novo and Dominantly Inherited <scp> SPTAN1 </scp> Mutations Cause Spastic Paraplegia and Cerebellar Ataxia

13. Ataxia And Cough Are Indicative For Biallelic RFC1 Repeat Expansions In Hereditary Sensory And Autonomic Neuropathy (S29.010)

14. RFC1 repeat expansions: A recurrent cause of sensory and autonomic neuropathy with cough and ataxia

15. RFC1 repeat expansions: A recurrent cause of sensory and autonomic neuropathy with cough and ataxia

16. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

17. De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies.

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