Fingerprint
Dive into the research topics of 'Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder
Mohammed Mohammed, Nadia Al-Hashmi, Samiya Al-Rashdi, Nashat Al-Sukaiti, Kawther Al-Adawi, Marwa Al-Riyami, Almundher Al-Maawali*
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
24
Citations
(Scopus)