Congenital Ichthyosis in Severe Type II Gaucher Disease with a Homozygous Null Mutation

Publisher: Karger

E-ISSN: 1661-7819|100|2|194-197

ISSN: 1661-7800

Source: Neonatology, Vol.100, Iss.2, 2011-04, pp. : 194-197

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content