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Journal description
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Details for article 12 of 13 found articles
| Title: |
Severe early onset retinitis pigmentosa in a Moroccan patient with Heimler syndrome due to novel homozygous mutation of PEX1 gene |
| Author: |
Ratbi, Ilham Jaouad, Imane Cherkaoui Elorch, Hamza Al-Sheqaih, Nada Elalloussi, Mustapha Lyahyai, Jaber Berraho, Amina Newman, William G. Sefiani, Abdelaziz |
| Appeared in: |
European journal of medical genetics |
| Paging: | Volume 59 (2016) nr. 10 pages 5 p. |
| Year: |
2016 |
| Contents: | |
| Publisher: |
Elsevier Masson SAS |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 12 of 13 found articles
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