Wrn Mutations in Werner Syndrome Patients: Genomic Rearrangements, Unusual Intronic Mutations and Ethnic-Specific Alterations

AuthID
P-003-58C
29
Author(s)
Lee, L
·
Nuernberg, G
·
Saha, B
·
Nuernberg, P
·
[+4]·
[+3]·
[+2]·
Poot, M
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Ippel, PF
·
Hoehn, H
·
Martin, GM
·
Kubisch, C
·
Oshima, J
Tipo de Documento
Article
Year published
2010
Publicado
in HUMAN GENETICS, ISSN: 0340-6717
Volume: 128, Número: 1, Páginas: 103-111 (9)
Indexing
Publication Identifiers
Pubmed: 20443122
SCOPUS: 2-s2.0-77954025436
Wos: WOS:000278737600009
Source Identifiers
ISSN: 0340-6717
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