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Mirhosseini–Holmes–Walton syndrome : ウィキペディア英語版 | Mirhosseini–Holmes–Walton syndrome
Mirhosseini–Holmes–Walton syndrome is a syndrome which involves retinal degeneration, cataract, microcephaly, and mental retardation. It was first characterized in 1972. The gene or genes involved have not yet been determined. There is some evidence that this syndrome has the same genetic cause as Cohen syndrome. ==References== 〔
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Mirhosseini–Holmes–Walton syndrome」の詳細全文を読む
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