Mutations underlying 3-Hydroxy-3-Methylglutaryl CoA Lyase deficiency in the Saudi population

Journal article

Open access

Peer reviewed

Moeenaldeen Al-Sayed, Faiqa Imtiaz, Osama A Alsmadi, Mohammed S Rashed and Brian F Meyer

BMC medical genetics, Vol.7(1), pp.86-86

16/12/2006

PMCID: PMC1764877

PMID: 17173698

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Title: Mutations underlying 3-Hydroxy-3-Methylglutaryl CoA Lyase deficiency in the Saudi population
Creators - without role: Moeenaldeen Al-Sayed - King Faisal Specialist Hospital & Research Centre
Faiqa Imtiaz - King Faisal Specialist Hospital & Research Centre
Osama A Alsmadi - King Faisal Specialist Hospital & Research Centre
Mohammed S Rashed - King Faisal Specialist Hospital & Research Centre
Brian F Meyer - King Faisal Specialist Hospital & Research Centre
Publication Details: BMC medical genetics, Vol.7(1), pp.86-86
Publisher: BioMed Central
Identifiers: 9914003108331
Academic Unit: King Faisal University; Alfaisal University
Language: English
Resource Type: Journal article