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Q33914630-0F8B3418-40BC-4AF7-B0C0-60EB249B4420
Q33914630-0F8B3418-40BC-4AF7-B0C0-60EB249B4420
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http://www.wikidata.org/entity/statement/Q33914630-0F8B3418-40BC-4AF7-B0C0-60EB249B4420
A Chinese family with Axenfeld-Rieger syndrome: report of the clinical and genetic findings
P2860
Q33914630-0F8B3418-40BC-4AF7-B0C0-60EB249B4420
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33914630-0F8B3418-40BC-4AF7-B0C0-60EB249B4420
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77ee1c0bfc518f65dcfbc81387a04b4d0291ba33
P2860
Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome.