Pages that link to "Q36007608"

The following pages link to A novel beta thalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3' end of IVS 2 (Q36007608):

Displaying 13 items.

• Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia (Q22010459) (← links)
• Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G (Q24290144) (← links)
• X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene (Q24540280) (← links)
• A T to G mutation in the polypyrimidine tract of the second intron of the human beta-globin gene reduces in vitro splicing efficiency: evidence for an increased hnRNP C interaction (Q24623054) (← links)
• Two-exon skipping within MLPH is associated with coat color dilution in rabbits (Q27335075) (← links)
• Mutations in the regions of the Rous sarcoma virus 3' splice sites: implications for regulation of alternative splicing (Q30452175) (← links)
• Variable deletion of exon 9 coding sequences in cystic fibrosis transmembrane conductance regulator gene mRNA transcripts in normal bronchial epithelium (Q35925248) (← links)
• Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problem (Q38916771) (← links)
• DNA haplotype distribution in Algerian beta thalassaemia patients. An extended evaluation by family studies and representative molecular characterization (Q39411068) (← links)
• The beta- and delta-thalassemia repository (Q44534771) (← links)
• First Report of the Rare IVS-II-705 (T>G) β-Thalassemia Mutation in a Chinese Family (Q49691237) (← links)
• Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A). (Q51013487) (← links)
• Genetic analysis of patients with leukocyte adhesion deficiency: genomic sequencing reveals otherwise undetectable mutations (Q77738099) (← links)