Marίa Eugenia Foncuberta

2PUBLICATIONS
22CO-AUTHORS
Neurology and neuromuscular diseasesNanomedicine
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Publications (2)

|Aug 18, 2026
Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin-Related Congenital Myopathy.

|Jun 11, 2022
Challenges in genetic diagnosis, co-occurrence of 22q11.2 deletion syndrome and Noonan syndrome.

Josefina Chinton, Victoria Huckstadt, Maria Eugenia Foncuberta

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Frequent Collaborators

1 joint publications

Josefina Chinton

1 joint publications

Victoria Huckstadt

1 joint publications

Luis Pablo Gravina

1 joint publications

María Gabriela Obregon