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A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy

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Year: 1995
Type: article
Source: Cell
DOI: 10.1016/0092-8674(95)90367-4
Authors: Brunella Franco, Germana Meroni, Giancarlo Parenti, Jacqueline Levilliers, Loris Bernard, Marinella Gebbia, Liza Cox, Pierre Maroteaux, Leslie Sheffield, Gudrun A Rappold, Generoso Andria, Christine Petit, Andrea Ballabio
Institutions: Baylor College of Medicine, University of Naples Federico II, Centre National de la Recherche Scientifique, Institut Pasteur, Hôpital Necker-Enfants Malades, Royal Children's Hospital, Heidelberg University, University of Siena
Language: English

Topic: Lysosomal Storage Disorders Research
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Institute of Neurological Disorders and Stroke
Awards: G5985072634, CLONING OF THE AICARDI AND GOLTZ SYNDROME GENES
OpenAlex ID: W1992386239
FWCI: 13.72
Cites: 50
Cited by: 314
Related to: 10
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