A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene
A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene
a_rare_case_of_deafness_2018.pdf
(Tampereen yliopisto - Trepo)
Tallennettuna:
| Kieli |
englanti |
|---|---|
| ISSN |
1415-4757 |