A rare case of familial multiple subcutaneous lipomatosis with novel PALB2 mutation and increased predilection to cancers
We describe the association of familial multiple subcutaneous lipomatosis with a PALB2 gene mutation (c.2716delT) and its increased predilection to cancers.
Kaydedildi:
| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Wolters Kluwer Medknow Publications
2016-10-01
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| Seri Bilgileri: | Hematology/Oncology and Stem Cell Therapy |
| Konular: | |
| Online Erişim: | https://journals.lww.com/10.1016/j.hemonc.2016.01.001 |
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