Severe congenital muscular dystrophy in a Mexican family with a new nonsense mutation (R2578X) in the laminin α-2 gene
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概要
- 論文の詳細を見る
- 2003-02-01
著者
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Mendoza Irma
メキシコ
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CORAL-VAZQUEZ Ramon
Unit of Medical Research in Human Genetics, Children's Hospital, XXI Century National Medical Center
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ROSAS-VARGAS Haydee
Unit of Medical Research in Human Genetics, Children's Hospital, XXI Century National Medical Center
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MEZA-ESPINOSA Pedro
Unit of Medical Research in Human Genetics, Children's Hospital, XXI Century National Medical Center
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MENDOZA Irma
Unit of Medical Research in Human Genetics, Children's Hospital, XXI Century National Medical Center
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HUICOCHEA Juan
Unit of Medical Research in Human Genetics, Children's Hospital, XXI Century National Medical Center
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RAMON Cuillermo
Pathology Department, Children's Hospital, XXI Century National Medical Center-IMSS
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SALAMANCA Fabio
Unit of Medical Research in Human Genetics, Children's Hospital, XXI Century National Medical Center
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Huicochea Juan
メキシコ
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Huicochea Juan
Unit Of Medical Research In Human Genetics Children's Hospital Xxi Century National Medical Cen
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Salamanca Fabio
メキシコ
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Salamanca Fabio
Unit Of Medical Research In Human Genetics Children's Hospital Xxi Century National Medical Cen
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Meza-espinosa Pedro
メキシコ
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Meza-espinosa Pedro
Unit Of Medical Research In Human Genetics Children's Hospital Xxi Century National Medical Cen
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Rosas-vargas Haydee
Unit Of Medical Research In Human Genetics Children's Hospital Xxi Century National Medical Cen
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Coral-vazquez Ramon
Unit Of Medical Research In Human Genetics Children's Hospital Xxi Century National Medical Cen
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Ramon Cuillermo
Pathology Department Children's Hospital Xxi Century National Medical Center-imss
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Mendoza Irma
Unit Of Medical Research In Human Genetics Children's Hospital Xxi Century National Medical Cen