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A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.

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Title: A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.
Authors: Liguori, Maria1,2 m.liguori@isn.cnr.it, La Russa, Antonella1, Manna, Ida1, Andreoli, Virginia1, Caracciolo, Manuela1, Spadafora, Patrizia1, Cittadella, Rita1, Quattrone, Aldo1,3
Source: Journal of Neurology. Jan2008, Vol. 255 Issue 1, p127-129. 3p. 1 Diagram.
Database: Academic Search Ultimate
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Header DbId: asn
DbLabel: Academic Search Ultimate
An: 28606315
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PubType: Academic Journal
PubTypeId: academicJournal
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  Data: A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Neurology%22">Journal of Neurology</searchLink>. Jan2008, Vol. 255 Issue 1, p127-129. 3p. 1 Diagram.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=28606315
RecordInfo BibRecord:
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    Identifiers:
      – Type: doi
        Value: 10.1007/s00415-008-0571-x
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      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 3
        StartPage: 127
    Titles:
      – TitleFull: A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.
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            NameFull: Liguori, Maria
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            NameFull: La Russa, Antonella
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            NameFull: Manna, Ida
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            NameFull: Andreoli, Virginia
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            NameFull: Caracciolo, Manuela
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            NameFull: Spadafora, Patrizia
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            – D: 01
              M: 01
              Text: Jan2008
              Type: published
              Y: 2008
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            – TitleFull: Journal of Neurology
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