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Article

No association between FGD1 gene polymorphisms and intellectual developmental disability in the Qinba mountain area.

Genetics and molecular research : GMR - 10 Jan 2014

Li J L, Li Y J, Zhang K J, Lan L, Shi J G, Yang X, Zhang M J, Zhang F C, Gao X C

Abstract excerpt

FGD1 encoding a guanine nucleotide exchange factor, specifically activates Rho GTPase cell division cycle 42 (Cdc42). Dysfunction of FGD1 causes Aarskog-Scott syndrome (MIM #305400), an X-linked disorder that may affect bone and intellectual development. However, the relationship between FGD1 and intellectual developmental disorders (IDD) remains unclear. The purpose of this study was to investigate the genetic...

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Source

Identifiers

PMID: 24446295
DOI: 10.4238/2014.January.10.3

Genes

FGD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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