Familial amyloidosis, light micrograph. Familial amyloidosis (also known as hereditary amyloidosis) results from mutations in the transthyretin gene. Abnormal transthyretin (ATTRm) accumulates as amyloid which is seen as amorphous pale pink deposits in the interstitium between the darker pink cardiac myocytes (muscle cells) in this image. | |
Licence : | Droits gérés |
Crédit: | Science Photo Library / WEBPATHOLOGY |
Taille de l’image : | 4096 px × 3200 px |
Model Release : | Non requis |
Property Release : | Non requis |
Restrictions : | - |