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DESCRIBE <http://purl.uniprot.org/SHA-384/8D6C2BCC401EE3ADC7D1C5B8AFCD4A203E83C241EA8305D7D664EF35FF6D37CECF998BD9C465E0EF399CE03302F71F89>
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http://purl.uniprot.org/SHA-384/8D6C2BCC401EE3ADC7D1C5B8AFCD4A203E83C241EA8305D7D664EF35FF6D37CECF998BD9C465E0EF399CE03302F71F89
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/8D6C2BCC401EE3ADC7D1C5B8AFCD4A203E83C241EA8305D7D664EF35FF6D37CECF998BD9C465E0EF399CE03302F71F89
http://www.w3.org/2000/01/rdf-schema#comment
"The study has found various mutations including deletions in CYP21A2 gene in Malaysian patients with 21-hydroxylase deficiency using the MLPA technique."
xsd:string
http://purl.uniprot.org/uniprot/#_2BB61417C00956714251C41C6F7E4ABF4AF8D9ECF9BF9D4350CDECCDF99173A6D538460265D4DCD7EEE3FAAC26622229
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/8D6C2BCC401EE3ADC7D1C5B8AFCD4A203E83C241EA8305D7D664EF35FF6D37CECF998BD9C465E0EF399CE03302F71F89
http://purl.uniprot.org/uniprot/B6VE01
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8D6C2BCC401EE3ADC7D1C5B8AFCD4A203E83C241EA8305D7D664EF35FF6D37CECF998BD9C465E0EF399CE03302F71F89
http://purl.uniprot.org/uniprot/#_B6VE01-mappedCitation-23027774
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8D6C2BCC401EE3ADC7D1C5B8AFCD4A203E83C241EA8305D7D664EF35FF6D37CECF998BD9C465E0EF399CE03302F71F89