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A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.
Zhang, K; Kniazeva, M; Han, M; Li, W; Yu, Z; Yang, Z; Li, Y; Metzker, M L; Allikmets, R; Zack, D J; Kakuk, L E; Lagali, P S; Wong, P W; MacDonald, I M; Sieving, P A; Figueroa, D J; Austin, C P; Gould, R J; Ayyagari, R; Petrukhin, K.
Affiliation
  • Zhang K; Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Nat Genet ; 27(1): 89-93, 2001 Jan.
Article in En | MEDLINE | ID: mdl-11138005
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Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Eye Proteins / Genes, Dominant / Macular Degeneration / Membrane Proteins Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals / Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 2001 Document type: Article Affiliation country: Country of publication:
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Eye Proteins / Genes, Dominant / Macular Degeneration / Membrane Proteins Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals / Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 2001 Document type: Article Affiliation country: Country of publication: