| 1 | Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy显示文摘To the Editor:Hypotrichosis with juvenile macular dystrophy(HJMD,OMIM:601553)is a rare autosomal recessive disorder characterized by short and sparse hair,progressive macular degeneration,decreased visual acuity,andevenblindness in early life. | Yunqing Ren Jipeng Liu Dianyi Yao Huixia Hua Xiaoxuan Guo Huatuo Dai Nan Dang Yan Huang Dianhe Yu | 2022 | Chinese Medical Journal2022，，12： | 0 |
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