Mutations in Snx14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

AuthID
P-009-ZMA
34
Author(s)
Thomas, AC
·
Williams, H
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Bacchelli, C
·
Jenkins, D
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O'Sullivan, M
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[+2]·
[+1]·
[+2]·
[+2]·
[+7]·
Houlden, H
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Hurst, J
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Bitner Glindzicz, M
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Moore, GE
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Stanier, P
Document Type
Article
Year published
2014
Published
in AMERICAN JOURNAL OF HUMAN GENETICS, ISSN: 0002-9297
Volume: 95, Issue: 5, Pages: 611-621 (11)
Indexing
Publication Identifiers
SCOPUS: 2-s2.0-84922281936
Wos: WOS:000344845000012
Source Identifiers
ISSN: 0002-9297
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Name Order Name   Name Order Name   Name Order Name
1 Thomas, AC;   2 Williams, H;   3 Seto Salvia, N;
4 Bacchelli, C;   5 Jenkins, D;   6 O'Sullivan, M;
7 Mengrelis, K;   8 Ishida, M;   9 Ocaka, L;
10 Chanudet, E;   11 James, C;   12 Lescai, F;
13 Anderson, G;   14 Morrogh, D;   15 Ryten, M;
16 Duncan, AJ;   17 Pai, YJ;   18 Saraiva, JM;
19 Ramos, F;   20 Farren, B;   21 Saunders, D;
22 Vernay, B;   23 Gissen, P;   24 Straatmaan Iwanowska, A;
25 Baas, F;   26 Wood, NW;   27 Hersheson, J;
28 Houlden, H;   29 Hurst, J;   30 Scott, R;
31 Bitner Glindzicz, M;   32 Moore, GE;   33 Sousa, SB;
34 Stanier, P;