Novel human pathological mutations. Gene symbol: LCA5. Disease: Leber congenital amaurosis

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Bibliographic Details
Published in:	Human genetics Vol. 127; no. 4; p. 487
Main Authors:	Vallespin, E, Avila-Fernandez, A, Almoguera, B, Velez-Monsalve, C, Cantalapiedra, D, Garcia-Hoyos, M, Riveiro-Alvarez, R, Aguirre-Lamban, J, Bustamante-Aragones, A, Trujillo-Tiebas, M J, Ayuso, C
Format:	Journal Article
Language:	English
Published:	Germany 01-04-2010
Subjects:	Amino Acid Substitution Base Sequence Codon - genetics Eye Proteins - genetics Humans Leber Congenital Amaurosis - genetics Microtubule-Associated Proteins - genetics Mutation, Missense
Online Access:	Get full text
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ISSN:	1432-1203