MYH9 is a large gene localized on chromosome 22q12.3-13.1 constituted of one 5ˊ-untranslated (exon 1) and 40 coding exons (Figure 1). It encodes for the heavy chain of the nonmuscle myosin IIA (NMM..
MYH9-related disease (MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, th...
Mutations of MYH9, the gene for non-muscle myosin heavy chain IIA (NMMHC-IIA), cause a complex clini...
MYH9-related disease (MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, th...
MYH9-related disease (MYH9-RD) is a rare autosomal dominant syndromic disorder caused by mutations i...
11siMYH9-related disease (MYH9-RD) is an autosomal-dominant thrombocytopenia caused by mutations in ...
The heterogeneous manifestations of MYH9‐related disorder (MYH9‐RD), characterized by macrothrombocy...
To improve the recognition of nonmuscle myosin heavy chain 9 gene (MYH9) mutations related disease.C...
MYH9-related disease (MYH9-RD) is a rare autosomal dominant syndromic disorder caused by mutations i...
MYH9-related disease (MYH9-RD) is a rare autosomal-dominant disorder caused by mutations in MYH9, th...
MYH9-related disease (MYH9-RD) is an autosomal-dominant thrombocytopenia caused by mutations in the ...
MYH9-related disease (MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, th...
Mutations of MYH9, the gene for non-muscle myosin heavy chain IIA (NMMHC-IIA), cause a complex clini...
MYH9-related disease (MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, th...
MYH9-related disease (MYH9-RD) is a rare autosomal dominant syndromic disorder caused by mutations i...
11siMYH9-related disease (MYH9-RD) is an autosomal-dominant thrombocytopenia caused by mutations in ...
The heterogeneous manifestations of MYH9‐related disorder (MYH9‐RD), characterized by macrothrombocy...
To improve the recognition of nonmuscle myosin heavy chain 9 gene (MYH9) mutations related disease.C...
MYH9-related disease (MYH9-RD) is a rare autosomal dominant syndromic disorder caused by mutations i...
MYH9-related disease (MYH9-RD) is a rare autosomal-dominant disorder caused by mutations in MYH9, th...
MYH9-related disease (MYH9-RD) is an autosomal-dominant thrombocytopenia caused by mutations in the ...
MYH9-related disease (MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, th...
Mutations of MYH9, the gene for non-muscle myosin heavy chain IIA (NMMHC-IIA), cause a complex clini...
MYH9-related disease (MYH9-RD) is a rare autosomal dominant disorder caused by mutations in MYH9, th...
DOI
Add to ORKG