Published August 31, 2015 | Version v1
Journal article

Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.

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Description

International audience

Additional details

Identifiers

URL
https://hal.science/hal-01218555
URN
urn:oai:HAL:hal-01218555v1

Origin repository

Origin repository
UNICA