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Identification of a SEDL gene mutation in an individual with Leber hereditary optic neuropathy and spondyloepiphyseal dysplasia

✍ Scribed by Marie A. Shaw; Barbara McDonough; Arthur B. Hodess; Donald H. Harter; Jozef Gécz


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
90 KB
Volume
129A
Category
Article
ISSN
1552-4825

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