Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia

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Bibliographic Details
Published in:Clinical genetics 2014, Vol.86 (5), p.500-501
Main Authors: Wakil, S M, Monies, D M, Ramzan, K, Hagos, S, Bastaki, L, Meyer, B F, Bohlega, S
Format: Report
Language:English
Online Access:Get full text
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ISSN:1399-0004
DOI:10.1111/cge.12312