Literature DB >> 16586002

Point mutation in the STS gene in a severely affected patient with X-linked recessive ichthyosis.

Luz M Gonzalez-Huerta, Olga M Messina-Baas, Jaime Toral-Lopez, María R Rivera-Vega, Susana Kofman-Alfaro, Sergio A Cuevas-Covarrubias.   

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Year:  2006        PMID： 16586002     DOI： 10.1080/00015550510043993

Source DB:  PubMed          Journal:  Acta Derm Venereol        ISSN： 0001-5555            Impact factor:   4.437


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  1 in total

1.  Pre-Descemet corneal dystrophy and X-linked ichthyosis associated with deletion of Xp22.31 containing the STS gene.

Authors:  Crystal Hung; Reed I Ayabe; Cynthia Wang; Ricardo F Frausto; Anthony J Aldave
Journal:  Cornea       Date:  2013-09       Impact factor: 2.651
  1 in total

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