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Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia
Journal article   Peer reviewed

Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia

S. M. Wakil, D. M. Monies, K. Ramzan, S. Hagos, L. Bastaki, B. F. Meyer and S. Bohlega
Clinical genetics, Vol.86(5), pp.500-501
01/11/2014
PMID: 24283893

Abstract

Genetics & Heredity Life Sciences & Biomedicine Science & Technology

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