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A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness

✍ Scribed by Felix Karl Jacobi; Christian P. Hamel; Bernard Arnaud; Nikolaus Blin; Martina Broghammer; Philipp C. Jacobi; Eckart Apfelstedt-Sylla; Carsten M. Pusch

Book ID: 117018852
Publisher: Elsevier Science
Year: 2003
Tongue: English
Weight: 191 KB
Volume: 135
Category: Article
ISSN: 0002-9394
DOI: 10.1016/s0002-9394(02)02109-8

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