Showing results 1 to 4 of 4
| Title | Author(s) | Issue Date | |
|---|---|---|---|
| 2020 | |||
Mutations in SEC24D cause autosomal recessive osteogenesis imperfecta Journal:Clinical Genetics | 2016 | ||
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement Journal:American Journal of Human Genetics | 2006 | ||
| 2019 |