Pages that link to "Q28264626"

The following pages link to Compound heterozygosity for an out-of-frame deletion and a splice site mutation in the LAMB3 gene causes nonlethal junctional epidermolysis bullosa (Q28264626):

Displaying 13 items.

• Laminins and human disease (Q34071975) (← links)
• Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris (Q34099095) (← links)
• Gene therapy in combination with tissue engineering to treat epidermolysis bullosa. (Q36425931) (← links)
• Epidermolysis bullosa. I. Molecular genetics of the junctional and hemidesmosomal variants (Q36930182) (← links)
• Do cell junction protein mutations cause an airway phenotype in mice or humans? (Q37836200) (← links)
• Therapies for inherited skin fragility disorders. (Q38444460) (← links)
• Revertant mosaicism in junctional epidermolysis bullosa due to multiple correcting second-site mutations in LAMB3 (Q41877944) (← links)
• Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. (Q42504368) (← links)
• A missense mutation (G1506E) in the adhesion G domain of laminin-5 causes mild junctional epidermolysis bullosa (Q44565268) (← links)
• A synonymous mutation in SPINK5 exon 11 causes Netherton syndrome by altering exonic splicing regulatory elements (Q62513320) (← links)
• A new mouse model of junctional epidermolysis bullosa: the LAMB3 628G>A knockin mouse (Q85886104) (← links)
• Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis (Q90481510) (← links)
• Truncated typeXVII collagen expression in a patient with non-herlitz junctional epidermolysis bullosa caused by a homozygous splice-site mutation (Q95721410) (← links)