Studying a rare disease: two novel cases of NPHS3 caused by mutations in PLCE1 | Neveen Soliman

Studying a rare disease: two novel cases of NPHS3 caused by mutations in PLCE1

Citation:: Studying a rare disease: two novel cases of NPHS3 caused by mutations in PLCE1, Hinkes, G., Chernin D., Heeringa S., Schoeb D., Bockenhauer D., Soliman N. A., Dotsch J., and Hildebrandt F. , PEDIATR NEPHROL, Volume 24, Number 4, p.904–904, (2009)

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