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Human Mutation, ISSN 1059-7794, 02/2014, Volume 35, Issue 2, pp. 236 - 247
Journal Article
Human Mutation, ISSN 1059-7794, 03/2008, Volume 29, Issue 3, pp. 409 - 417
Journal Article
American Journal of Hematology, ISSN 0361-8609, 06/2019, Volume 94, Issue 6, pp. 667 - 677
MYH9 ‐related disease ( MYH9 ‐RD) is a rare, autosomal dominant disorder caused by mutations in MYH9 , the gene encoding the actin‐activated motor protein... 
LYTIC GRANULES | F-ACTIN | ERYTHROCYTES | CRYSTAL-STRUCTURE | MACROTHROMBOCYTOPENIA | NONMUSCLE | MYH9 | ENUCLEATION | IDENTIFICATION | HEMATOLOGY | ELLIPTOCYTOSIS | Spectrin | Cataracts | Deafness | Phenotypes | Deformability | Blood cells | Erythrocytes | Cytology | Blood | Hereditary diseases | Filaments | Actin | Myosin | Peripheral blood | Hemoglobin | Mutation | Kidney diseases
Journal Article
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia, 04/2017, Volume 34, Issue 2, pp. 40 - 57
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 2012, Volume 56, Issue 1, pp. 7 - 12
Journal Article
Journal Article
03/2012
Hematopoiesis is an intricately regulated homeostatic process that maintains all of the differentiated blood cell lineages. N-ethyl-N-nitrosurea (ENU) is a... 
5-fluorouracil | 0369 | Forward Genetic Screen | n-ethyl-n-nitrosurea | Hematopoiesis | Hereditary Spherocytosis | 0719 | Myh9 Related Disease | 0306
Dissertation
Journal Article
Genomics, ISSN 0888-7543, 06/2004, Volume 83, Issue 6, pp. 1125 - 1133
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 11/2010, Volume 363, Issue 21, pp. 2058 - 2059
Journal Article
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 09/2018, Volume 16, Issue 9, pp. 1700 - 1710
Journal Article