Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan

Autor:	Khan, M., Ajmal, M., Micheal, S., Azam, M., Hussain, A., Shahzad, A., Venselaar, H., Bokhari, H., Wijs, I.J. de, Hoefsloot, L.H., Waheed, N., Collin, R.W.J., Hollander, A.I. den, Qamar, R., Cremers, F.P.M.
Rok vydání:	2013
Předmět:	Chemical and physical biology [NCMLS 7] Genetics and epigenetic pathways of disease [NCMLS 6] Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6]
Zdroj:	Clinical Genetics, 84, 290-3 Clinical Genetics, 84, 3, pp. 290-3
ISSN:	0009-9163
Popis:	Contains fulltext : 118540.pdf (Publisher’s version ) (Closed access)
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d9a8e52178eddca93e8268306e986915 https://hdl.handle.net/2066/118540 Zobrazit plný text záznamu Plný text