Blau syndrome with a rare mutation in exon 9 of [electronic resource]
Producer: 20200702Description: 256-263 p. digitalISSN:- 1607-842X
- Adult
- Alleles
- Arthritis -- diagnosis
- Child
- Dermatitis -- diagnosis
- Exons
- Female
- Gene Expression
- Granulomatous Disease, Chronic -- diagnosis
- Headache -- diagnosis
- High-Throughput Nucleotide Sequencing
- Humans
- Male
- Middle Aged
- Mutation, Missense
- Nod2 Signaling Adaptor Protein -- genetics
- Sarcoidosis
- Stroke -- diagnosis
- Synovitis -- diagnosis
- Uveitis -- diagnosis
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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