A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy-Reference-Cited by-同舟云学术

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

Published:1995-04 Issue:1 Volume:81 Page:15-25
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Franco Brunella,Meroni Germana,Parenti Giancarlo,Levilliers Jacqueline,Bernard Loris,Gebbia Marinella,Cox Liza,Maroteaux Pierre,Sheffield Leslie,Rappold Gudrun A,Andria Generoso,Petit Christine,Ballabio Andrea

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference48 articles.

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2. Steroid sulfatase deficiency and X-linked ichthyosis;Ballabio,1995

3. Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency;Ballabio;Hum. Genet.,1985

4. Isolation and characterization of a steroid sulphatase cDNA clone: genomic deletions in patients with X chromosome-linked ichthyosis;Ballabio,1987

5. Characterization of a murine gene expressed from the inactive X chromosome;Borsani;Nature,1991

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