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Posterior chorioretinal atrophy and vitreous phenotype in a family with Stickler syndrome from a mutation in the COL2A1 gene

✍ Scribed by Cuong D Vu; Jeremiah Brown Jr.; Jarmo Körkkö; Robert Ritter III; Albert O Edwards

Book ID
115548759
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
501 KB
Volume
110
Category
Article
ISSN
0161-6420

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