dynamin 2 การใช้

• This condition is now known as dynamin 2 centronuclear myopathy ( abbreviated DNM2-CNM ).
• Additionally, the protein has binding sites for endophilin 3 and dynamin 2 at amino acids 89-100 and 195-214, respectively.
• Recently, researchers discovered mutations at the gene dynamin 2 ( DNM2 on chromosome 19, at site 19p13.2 ), responsible for the autosomal dominant form of centronuclear myopathy.