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Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 gene.
Am J Hum Genet. 1999 Jul;65(1):68-76. doi: 10.1086/302443.
Am J Hum Genet. 1999.
PMID: 10364518
Free PMC article.
OCRL1 mutation analysis in French Lowe syndrome patients: implications for molecular diagnosis strategy and genetic counseling.
Monnier N, Satre V, Lerouge E, Berthoin F, Lunardi J.
Monnier N, et al. Among authors: berthoin f.
Hum Mutat. 2000;16(2):157-65. doi: 10.1002/1098-1004(200008)16:2<157::AID-HUMU8>3.0.CO;2-9.
Hum Mutat. 2000.
PMID: 10923037
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