Vohwinkel syndrome with De novo mutation in the GJB2 gene with Heterozygous mutation c.175G>A (p. Gly59Ser).

IF 2.6 4区 医学 Q2 DERMATOLOGY
María Caridad Duran-Lemarie, Luis Enrique Cano-Aguilar, Edmar Obed Benitez-Alonso, Dalia Cruz-Sotomayor, Ulises Villela-Segura, Hector Proy-Trujillo
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引用次数: 0
Vohwinkel 综合征,GJB2 基因从头突变,杂合突变 c.175G>A (p. Gly59Ser)。
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来源期刊
CiteScore
2.40
自引率
0.00%
发文量
184
审稿时长
32 days
期刊介绍: The journal is published bimonthly and is devoted to the dissemination of original, unpublished technical-scientific study, resulting from research or reviews of dermatological topics and related matters. Exchanges with other publications may be accepted.
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