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Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia
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Published in: | Clinical genetics 2014, Vol.86 (5), p.500-501 |
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Main Authors: | , , , , , , |
Format: | Report |
Language: | English |
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container_end_page | 501 |
container_issue | 5 |
container_start_page | 500 |
container_title | Clinical genetics |
container_volume | 86 |
creator | Wakil, S M Monies, D M Ramzan, K Hagos, S Bastaki, L Meyer, B F Bohlega, S |
description | |
doi_str_mv | 10.1111/cge.12312 |
format | report |
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fulltext | fulltext |
identifier | EISSN: 1399-0004 |
ispartof | Clinical genetics, 2014, Vol.86 (5), p.500-501 |
issn | 1399-0004 |
language | eng |
recordid | cdi_proquest_miscellaneous_1613940086 |
source | Wiley-Blackwell Read & Publish Collection |
title | Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia |
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