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Annual Report Collection

 2012

 A novel tyrosine 516 stop mutation in the α subunit of the epithelial sodium channel causing Pseudohypoaldosteronism in the affected offspring and A subclinical, saltlosing phenotype in a heterozygous mother

 Zahrani, Ahmad

//uquui/handle/20.500.12248/129975
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dc.contributor.authorZahrani, Ahmad-
dc.date.accessioned2020-10-12T06:53:18Z-
dc.date.available2020-10-12T06:53:18Z-
dc.date.issued2012en_US
dc.identifier.urihttps://dorar.uqu.edu.sa/uquui/handle/20.500.12248/129975-
dc.language.isoانجليزيen_US
dc.relation.isformatofمجلة جامعة أم القرى الطبيةen_US
dc.subjectBlood Diseasesen_US
dc.titleA novel tyrosine 516 stop mutation in the α subunit of the epithelial sodium channel causing Pseudohypoaldosteronism in the affected offspring and A subclinical, saltlosing phenotype in a heterozygous motheren_US
dc.title.alternativeطفرة غير مألوفة في وحيدة الفا في قنوات الصوديوم الطلائية مسببة لمرض الالدوستيرون الكاذب عند امen_US
dc.type.formatمقالen_US
dc.date.issuedhijri1432en_US
dc.description.extentTen pagesen_US
dc.relation.issueUQU Medical Journalen_US
Appears in Collections :مجلة جامعة ام القرى الطبية

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