Find in Library
Search millions of books, articles, and more
Indexed Open Access Databases
H syndrome: A rare case with homozygous mutation in SLC29A3 gene
oleh: Sahana M Srinivas, Sowjanya G Thimmaiah, Radha Venkatesan, Raghupathy Palany
| Format: | Article |
|---|---|
| Diterbitkan: | Wolters Kluwer Medknow Publications 2020-01-01 |
Deskripsi
No description available for this item.