Corrigendum: Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus (Human Molecular Genetics (2000) 9 (367-374))

Human Molecular Genetics

Volumn 9, Issue 7, 2000, Pages 1141-

  Bejjani, B A ^a   Stockton, D W ^a   Lewis, R A ^a   Tomey, K F ^a   Dueker, D K ^a   Jabak, M ^a   Astle, W F ^a   Lupski, J R ^a  

^a NONE

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ARTICLE; ERROR; PRIORITY JOURNAL;

EID: 0034639934     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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