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usherin
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USH2A — Usher syndrome 2A (autosomal recessive, mild), also known as USH2A, is a human gene. PBB Summary section title = summary text = This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs … Wikipedia
Usher syndrome — Classification and external resources OMIM 276900 276901 DiseasesDB 13611 … Wikipedia
Harmonin — Masse/Länge Primärstruktur 552 Aminosäuren … Deutsch Wikipedia
Usher-Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie H90.3 … Deutsch Wikipedia
Usher Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie … Deutsch Wikipedia
Usher syndrome — noun A relatively rare genetic disorder that is a leading cause of deafblindness. Syn: Hallgren syndrome See Also: usherin … Wiktionary
Síndrome de Usher — Clasificación y recursos externos OMIM 276900 … Wikipedia Español
Usherina — Símbolo USH2A Símbolos alt. US2; USH2; dJ1111A8.1 Datos genéticos Código de gen USH2A … Wikipedia Español
