Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder

标题
Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder
作者
关键词
Hermansky-Pudlak syndrome, Immunodeficiency, Seizures, AP3D1
出版物
European Journal of Medical Genetics
Volume -, Issue -, Pages -
出版商
Elsevier BV
发表日期
2018-11-23
DOI
10.1016/j.ejmg.2018.11.017

向作者/读者发起求助以获取更多资源

Reprint

联系作者

Find Funding. Review Successful Grants.

Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.

Explore

Publish scientific posters with Peeref

Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.

Learn More