A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E - Concepedia

Concepedia

Publication | Closed Access

A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E

57

Citations

22

References

2007

Year

Laurence Jonard, Delphine Feldmann, Christophe Parsy, Sylvie Freitag, Martine Sinico, Céleste Koval, M’hamed Grati, Rémy Couderc, Françoise Denoyelle, Christine Bodemer,

European Journal of Medical Genetics

Mendelian DisorderGenetic DisorderInherited Metabolic DiseasePediatricsDermatologyFamilial CaseSclerodermaMedicineGjb2 Mutation G45eInborn Error Of ImmunityClinical Genetics

References

	Year	Citations

Page 1

Page 1