Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis.
Regina C. Betz(University Hospital Bonn), Friedhelm Hildebrandt(Boston Children's Hospital), Edgar A. Otto(University of Michigan), Christopher Rensing(Fujian Agriculture and Forestry University), Peter Lichter(German Cancer Research Center), Antoaneta Mincheva(University of Freiburg)
PubMed
June 1, 2000
Cited by 88
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