Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome). (Q33335770)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome). |
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Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome) (English)
S Kunishima
T Kojima
T Matsushita
M Tsurusawa
Y Furukawa
Y Nakamura
T Okamura
N Amemiya
T Nakayama
T Kamiya