MULTIPLE GNAS1, FGF23, FGFR3 GENES' STRIKING MUTATIONS IN CKD PATIENTS WITH SH. NEW BONE DISPLASIA-HEREDITARY OSTEODISTROPHY AND UGLIFYING HUMAN FACE APPEARANCES. SAGLIKER SYNDROME
Nephrology Dialysis Transplantation（2017）
Key words
fgfr3 genes,fgf23,uglifying human face appearances,mutations,displasia-heredi
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined