Carrier Assessment in Families with Lowe Oculocerebrorenal Syndrome: Novel Mutations in the OCRL1 Gene and Correlation of Direct DNA Diagnosis with Ocular Examination
Wulf Röschinger, Ania C. Muntau, Günther Rudolph, Adelbert A. Roscher, Stefan KammererVolume:
69
Year:
2000
Language:
english
Pages:
223
DOI:
10.1006/mgme.1999.2955
File:
PDF, 228 KB
english, 2000