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A clinical and genetic study of 56 Saudi Wilson disease patients: identification of Saudi-specific mutations.
Al Jumah, M; Majumdar, R; Al Rajeh, S; Awada, A; Al Zaben, A; Al Traif, I; Al Jumah, A R; Rehana, Z.
Affiliation
  • Al Jumah M; Section of Neurology, Department of Medicine, King Fahad National Guard Hospital, Riyadh, Saudi Arabia. jumahm@ngha.med.sa
Eur J Neurol ; 11(2): 121-4, 2004 Feb.
Article in En | MEDLINE | ID: mdl-14748773
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Adenosine Triphosphatases / Cation Transport Proteins / Hepatolenticular Degeneration / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2004 Document type: Article Affiliation country:
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Adenosine Triphosphatases / Cation Transport Proteins / Hepatolenticular Degeneration / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2004 Document type: Article Affiliation country: