Výsledky vyhledávání - "Brooke Weckselbatt"

DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia

Autor: Aiko Iwata-Otsubo, Kosuke Izumi, Brooke Weckselbatt, David Burgess, Alyssa Ritter, Laura K. Conlin, Nicole Ryan

Publikováno v: American journal of medical genetics. Part A. 176(1)

Dedicator of cytokinesis (DOCK) family are evolutionary conserved guanine nucleotide exchange factors (GEFs) for the Rho GTPases, Rac, and Cdc42. DOCK3 functions as a GEF for Rac1, and plays an important role in promoting neurite and axonal growth by

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0188a37c5a59617b19fe4355fafa15a1
https://pubmed.ncbi.nlm.nih.gov/29130632

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