Nemaline body myopathy caused by a novel mutation in troponin T1 (TNNT1 )

Author:

Abdulhaq Ulla Najwa1,Daana Mohannad1,Dor Talia1,Fellig Yakov2,Eylon Sharon3,Schuelke Markus4,Shaag Avraham5,Elpeleg Orly5,Edvardson Simon15

Affiliation:

1. Department of Pediatrics; Hadassah-Hebrew University Medical Center; Jerusalem Israel

2. Department of Pathology Hadassah-Hebrew University Medical Center; Jerusalem Israel

3. Alyn Hospital Pediatric and Adolescent Rehabilitation Center; Jerusalem Israel

4. Klinik für Pädiatrie Neurologie and NeuroCure Clinical Research Center, Charité-Universitätsmedizin; Berlin Germany

5. Monique and Jacques Roboh Department of Genetic Research; Hadassah-Hebrew University Medical Center; Jerusalem Israel

Funder

Einstein Stiftung Berlin

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

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