Mutations in Progranulin Gene: Clinical, Pathological, and Ribonucleic Acid Expression Findings
✍ Scribed by Adolfo López de Munain; Ainhoa Alzualde; Ana Gorostidi; David Otaegui; Javier Ruiz-Martínez; Begoña Indakoetxea; Isidro Ferrer; Jordi Pérez-Tur; Amets Sáenz; Alberto Bergareche; Miriam Barandiarán; Juan José Poza; Ramón Zabalza; Irune Ruiz; Miguel Urtasun; Iñaki Fernández-Manchola; Bixen Olasagasti; Juan Bautista Espinal; Javier Olaskoaga; Marta Ruibal; Fermin Moreno; Nieves Carrera; José Félix Martí Massó
- Book ID
- 119197715
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 439 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0006-3223
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Reports on Noonan syndrome (NS) have documented multiple types of coagulation defects and bleeding diathesis, and a wide range of clinical presentations. Early studies suggested that a large proportion of NS patients have coagulation defects, whereas more recent reports indicate low rat