Michele Boniotto

3PUBLICATIONS
2CO-AUTHORS
Developmental genetics (incl. sex determination)Neurology and neuromuscular diseasesDemography not elsewhere classified
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Publications (3)

|Sep 04, 2023
A loss-of-function NCSTN mutation associated with familial Dowling Degos disease and hidradenitis suppurativa.

Ana Sofia Lima Estevao de Oliveira, Roberta Cardoso de Siqueira, Cécile Nait-Meddour

|Sep 08, 2020
Comorbid acne inversa and Dowling-Degos disease due to a single NCSTN mutation: is there enough evidence? Reply from the authors.

S Garcovich, P M Tricarico, C N Meddour

|Apr 14, 2020
Novel nicastrin mutation in hidradenitis suppurativa-Dowling-Degos disease clinical phenotype: more than just clinical overlap?

S Garcovich, P M Tricarico, C Nait-Meddour

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Frequent Collaborators

2 joint publications

S Garcovich

1 joint publications

Ana Sofia Lima Estevao de Oliveira