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1.
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome.
J Med Genet
; 61(5): 490-501, 2024 Apr 19.
Article
in English
| MEDLINE | ID: mdl-38296633
2.
Sequence and structural variations determining the recruitment of WNK kinases to the KLHL3 E3 ligase.
Biochem J
; 479(5): 661-675, 2022 03 18.
Article
in English
| MEDLINE | ID: mdl-35179207
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