Amish nemaline myopathy is an autosomal recessive disorder caused by mutations of the TNNT1 gene.
1. |
Johnston JJ et al. (2000) A novel nemaline myopathy in the Amish caused by a mutation in troponin T1. |
2. |
OMIM.ORG article Omim 605355 |
3. |
Orphanet article Orphanet ID 98902 |
4. |
Wikipedia article Wikipedia EN (Nemaline_myopathy) |