Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome
- PMID: 15286156
- PMCID: PMC1735873
- DOI: 10.1136/jmg.2004.019661
Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome
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