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Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome
- Correspondence to: Dr Ghosh Institute of Child Health, 11 Dr Biresh Guha Street, Calcutta 700017, India; apurbaghoshyahoo.com Dr Heinimann Research Group Human Genetics, Division of Medical Genetics, University Children’s Hospital, Roemergasse 8, 4005 Basel, Switzerland; karl.heinimannunibas.ch
Citation
Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome
Publication history
- Received March 12, 2004
- Accepted March 12, 2004
- First published July 30, 2004.
Online issue publication
April 27, 2016
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Copyright 2004 Journal of Medical Genetics