Work

Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum

Year: 2010

Type: article

Source: Clinical Genetics

DOI: 10.1111/j.1399-0004.2010.01513.x

Authors: M Castori, D Castiglia, F Brancati, M Foglio, S Heath, G Floriddia, S Madonna, J Fischer, G Zambruno

Institutions: Azienda Ospedaliera San Camillo-Forlanini, Sapienza University of Rome, Istituto Dermopatico dell'Immacolata, Istituti di Ricovero e Cura a Carattere Scientifico, University of Chieti-Pescara, Commissariat à l'Énergie Atomique et aux Énergies Alternatives

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

OpenAlex ID: W1994925426

FWCI: 0.996

Cites: 16

Cited by: 23

Related to: 10