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- [43] X-linked Retinoschisis Associated with Retinitis Punctata Albescens Caused by a Mutation in the RS1 Gene: A Family Study OPEN OPHTHALMOLOGY JOURNAL, 2021, 15 : 201 - 205
- [49] Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypo-gonadotropic hypogonadism from India NATIONAL MEDICAL JOURNAL OF INDIA, 2019, 32 (03): : 141 - 143