Hasil Pencarian - Paulina Bahena
- Menampilkan 1 - 2 hasil dari 2
-
1
A novel missense variant in MYO3A is associated with autosomal dominant high‐frequency hearing loss in a German family oleh Julia Doll, Michaela A. H. Hofrichter, Paulina Bahena, Alfred Heihoff, Dennis Segebarth, Tobias Müller, Marcus Dittrich, Thomas Haaf, Barbara Vona
Diterbitkan 2020-08-01Dapatkan teks lengkap
Artikel -
2
Expanding the clinical phenotype of IARS2-related mitochondrial disease oleh Barbara Vona, Reza Maroofian, Emanuele Bellacchio, Maryam Najafi, Kyle Thompson, Ahmad Alahmad, Langping He, Najmeh Ahangari, Abolfazl Rad, Sima Shahrokhzadeh, Paulina Bahena, Falk Mittag, Frank Traub, Jebrail Movaffagh, Nafise Amiri, Mohammad Doosti, Reza Boostani, Ebrahim Shirzadeh, Thomas Haaf, Daria Diodato, Miriam Schmidts, Robert W. Taylor, Ehsan Ghayoor Karimiani
Diterbitkan 2018-11-01Dapatkan teks lengkap
Artikel