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Article

HOXA1 mutations are not a common cause of Duane anomaly.

American journal of medical genetics. Part A - 15 Apr 2006

Tischfield Max A, Chan Wai-Man, Grunert Jann-Frederik, Andrews Caroline, Engle Elizabeth C

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Share to Amino Acid Substitution
Share to Homeodomain Proteins
Share to Mutation
Share to Polymorphism, Single Nucleotide

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 16528738
DOI: 10.1002/ajmg.a.31167
PMCID: PMC2553396

Genes

HOXA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

HOXA1 mutations are not a common cause of Duane anomaly.PMID 16528738Read ↗

A novel duplication in the HOXA13 gene in a family with atypical hand-foot-genital syndrome.Semantic proximity Read ↗

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Mutations in HOXA11 are not responsible for Müllerian duct anomalies in Chinese patients.Semantic proximity Read ↗

Human HOX gene mutations.Semantic proximity Read ↗

The 4 bp deletion mutation in HOXD1 gene determines the polycerate trait in Chinese Sishui fur sheep.Semantic proximity Read ↗

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Ucma is not necessary for normal development of the mouse skeletonSemantic proximity Read ↗

Identification of a HOXD13 mutation in a VACTERL patient.Semantic proximity Read ↗

CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome.Semantic proximity Read ↗

Mutations in SURF1 are not specifically associated with Leigh syndrome.Semantic proximity Read ↗

A HOX Gene Mutation in a Family with Isolated Congenital Vertical Talus and Charcot-Marie-Tooth DiseaseSemantic proximity Read ↗

The Wnt signalling ligand RSPO4, causing inherited anonychia, is not mutated in a patient with congenital nail hypoplasia/aplasia with underlying skeletal defects.Semantic proximity Read ↗

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