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Output details

5 - Biological Sciences

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Article title

Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia

Type

D - Journal article

DOI

Title of journal

American Journal of Human Genetics

Article number

Volume number

Issue number

First page of article

965

ISSN of journal

0002-9297

Year of publication

2013

URL

Number of additional authors

Additional information

Interdisciplinary

Cross-referral requested

Research group

None

Citation count

Proposed double-weighted

Double-weighted statement

Reserve for a double-weighted output

Non-English

English abstract