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Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15

✍ Scribed by F. Yesim K. Demirci; Nisha Gupta; Amy L. Radak; Brian W. Rigatti; Tammy S. Mah; Ann H. Milam; Michael B. Gorin

Book ID: 116200005
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 240 KB
Volume: 139
Category: Article
ISSN: 0002-9394
DOI: 10.1016/j.ajo.2004.08.041

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