A sibling pair with autosomal recessive Charcot–Marie–Tooth disease due to novel ganglioside-induced differentiation-associated protein 1 mutation
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2017-01-01
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| Series: | Annals of Indian Academy of Neurology |
| Online Access: | http://www.annalsofian.org/article.asp?issn=0972-2327;year=2017;volume=20;issue=4;spage=434;epage=435;aulast=Shah |