Case Report
Published on 31 Oct 2019
Hereditary Sensory and Autonomic Neuropathy 2B Caused by a Novel RETREG1 Mutation (c.765dupT) and Paternal Uniparental Isodisomy of Chromosome 5
in Genetics of Common and Rare Diseases
- 2,983 views
- 10 citations
Case Report
Published on 31 Oct 2019
in Genetics of Common and Rare Diseases
Brief Research Report
Published on 29 Oct 2019
in Genetics of Common and Rare Diseases
Original Research
Published on 29 Oct 2019
in Genetics of Common and Rare Diseases
Original Research
Published on 29 Oct 2019
in Genetics of Common and Rare Diseases
Original Research
Published on 22 Oct 2019
in Genetics of Common and Rare Diseases
Original Research
Published on 22 Oct 2019
in Genetics of Common and Rare Diseases
Original Research
Published on 08 Oct 2019
in Genetics of Common and Rare Diseases
Case Report
Published on 02 Oct 2019
in Genetics of Common and Rare Diseases
Case Report
Published on 27 Sep 2019
in Genetics of Common and Rare Diseases
Review
Published on 25 Sep 2019
in Genetics of Common and Rare Diseases
Brief Research Report
Published on 24 Sep 2019
in Genetics of Common and Rare Diseases
Original Research
Published on 20 Sep 2019
in Genetics of Common and Rare Diseases
Brief Research Report
Published on 20 Sep 2019
in Genetics of Common and Rare Diseases
Original Research
Published on 18 Sep 2019
in Genetics of Common and Rare Diseases
Original Research
Published on 18 Sep 2019
in Genetics of Common and Rare Diseases
Original Research
Published on 18 Sep 2019
in Genetics of Common and Rare Diseases