scholarly article | Q13442814 |
P356 | DOI | 10.1089/GTE.2007.0026 |
P698 | PubMed publication ID | 18373399 |
P50 | author | Huixia Yang | Q56424320 |
P2093 | author name string | Fang Wang | |
Jie Ding | |||
Hongwen Zhang | |||
P433 | issue | 1 | |
P921 | main subject | Alport syndrome | Q1331116 |
P304 | page(s) | 1-7 | |
P577 | publication date | 2008-03-01 | |
P1433 | published in | Genetic Testing and Molecular Biomarkers | Q15753742 |
P1476 | title | Prenatal diagnosis and genetic counseling of a Chinese Alport syndrome kindred. | |
P478 | volume | 12 |
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Q46036955 | Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patients. |
Q38647928 | Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing |
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