Nemaline body myopathy caused by a novel mutation in troponin T1 (TNNT1 )-Reference-Cited by-同舟云学术

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

Link

Reference16 articles.

1. Nemaline myopathies;Wallgren-Pettersson;Semin Pediatr Neurol,2011

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