// App-Quantinova.ai

TP0947 : Normal NFKB2 gene by sanger sequencing in a patient with hypogammaglobulinaemia, alopecia and central adrenal insufficiency

Researchers

Presenter

  • Tadros S

Principal Investigators

  • Martini H

  • Verma N

  • Karafotias I

  • Sundaram K

  • Gross-Kreul D

  • Gooi H

  • Adhya Z

  • Ibrahim M

Medical Centers

  • King's College Hosptial NHS Foundation Trust, London, United Kingdom

Locations

  • United Kingdom

Companies

  • N/A

Study Components

Therapeutic Area

  • Endocrine/metabolic Diseases (ME)

Disease

  • Hypogammaglobulinaemia

  • Addison's disease

Biomarkers

  • N/A

Drug/Treatment

  • N/A

Outcome

  • N/A


Study Design

  • N/A

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • N/A