Identification of Two Novel ANKRD11 Mutations: Highlighting Incomplete Penetrance in KBG Syndrome.

Authors :: Amllal N
Elalaoui SC
Zerkaoui M
Chiguer A
Afif L
Izgua AT
Sefiani A
Lyahyai J
Source :: Annals of laboratory medicine [Ann Lab Med] 2024 Jan 01; Vol. 44 (1), pp. 110-117. Date of Electronic Publication: 2023 Sep 04.
Publication Year :: 2024

Subjects :: Humans
Facies
Penetrance
Mutation
Repressor Proteins genetics
Abnormalities, Multiple
Intellectual Disability
Bone Diseases, Developmental
Tooth Abnormalities

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