共 50 条
- [22] Ophthalmic phenotype of TCIRG1 gene mutations in Chinese infantile malignant osteopetrosis BMJ OPEN OPHTHALMOLOGY, 2018, 3 (01):
- [24] Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis Nature Genetics, 2000, 25 : 343 - 346
- [26] RARE GROSS DELETION IN TCIRG1 GENE IN IRANIAN FAMILY WITH INFANTILE MALIGNANT OSTEOPETROSIS HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 : 532 - 532
- [27] RARE GROSS DELETION IN TCIRG1 GENE IN IRANIAN FAMILY WITH INFANTILE MALIGNANT OSTEOPETROSIS HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2010, 95 : 679 - 680
- [28] RARE GROSS DELETION IN TCIRG1 GENE IN IRANIAN FAMILY WITH INFANTILE MALIGNANT OSTEOPETROSIS HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 : 494 - 494