Detalhe da pesquisa
1.
Heterozygous CAPN3 missense variants causing autosomal-dominant calpainopathy in seven unrelated families.
Neuropathol Appl Neurobiol
; 47(2): 283-296, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32896923
2.
Hereditary inclusion body myopathy in Persian Jews: a case report from Iran.
Clin Genet
; 85(6): 595-7, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23841835
3.
An Iranian family with congenital myasthenic syndrome caused by a novel acetylcholine receptor mutation (CHRNE K171X).
J Neurol Neurosurg Psychiatry
; 76(7): 1039-40, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15965226