Work

Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia

Year: 2007

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/ng2057

Authors: Xiaoling Wang, V Reid Sutton, J Omar Peraza-Llanes, Zhiyin Yu, Rebecca Rosetta, Ying-Chuck Kou, Tanya N Eble, Ankita Patel, Christina Thaller, Ping Fang, Ignatia B Van den Veyver

Institutions: Baylor College of Medicine, Mexican Social Security Institute

Language: English

Topic: Genetic and rare skin diseases.

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1179207774, Baylor Intellectual and Developmental Disabilities Research Center, New strategies to identify the gene mutated in Aicardi syndrome, G7880062387

OpenAlex ID: W1973982607

FWCI: 10.75

Cites: 15

Cited by: 283

Related to: 10