Novel human pathological mutations. Gene symbol: GUCY2D. Disease: Leber congenital amaurosis

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Bibliographic Details
Published in:	Human genetics Vol. 125; no. 3; p. 349
Main Authors:	Auz-Alexandre, Carmen-Laura, Vallespin, E, Aguirre-Lamban, J, Cantalapiedra, D, Avila-Fernandez, A, Villaverde-Montero, C, Ainse, E, Trujillo-Tiebas, M J, Ayuso, C
Format:	Journal Article
Language:	English
Published:	Germany 01-04-2009
Subjects:	Amino Acid Substitution Blindness - congenital Blindness - genetics Codon - genetics Guanylate Cyclase - genetics Humans Molecular Sequence Data Mutation, Missense Optic Atrophy, Hereditary, Leber - genetics Receptors, Cell Surface - genetics
Online Access:	Get full text
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Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	1432-1203