Null mutations in LTBP2 cause primary congenital glaucoma

Manir Ali; Martin McKibbin; Adam Booth; David Parry; Payal Jain; Amer Riazuddin; J Hejtmancik; Shaheen Khan; Sabika Firasat; Mike Shires; David Gilmour; Katherine Towns; Anna-Louise Murphy; Dimitar Azmanov; Ivailo Tournev; Sylvia Cherninkova; Hussain Jafri; Yasmin Raashid; C Toomes; Jamie Craig; David Mackey; Luba Kalaydjieva; Sheikh Riazuddin; C Inglehearn

Null mutations in LTBP2 cause primary congenital glaucoma

Manir Ali, Martin McKibbin, Adam Booth, David Parry, Payal Jain, Amer Riazuddin, J Hejtmancik, Shaheen Khan, Sabika Firasat, Mike Shires, David Gilmour, Katherine Towns, Anna-Louise Murphy, Dimitar Azmanov, Ivailo Tournev, Sylvia Cherninkova, Hussain Jafri, Yasmin Raashid, C Toomes, Jamie CraigDavid Mackey, Luba Kalaydjieva, Sheikh Riazuddin, C Inglehearn

Research output: Contribution to journal › Article › peer-review

261 Citations (Scopus)

Original language	English
Pages (from-to)	664-671
Number of pages	8
Journal	American Journal of Human Genetics
Volume	84
Issue number	5
Publication status	Published - 2009

Cite this

Ali, M., McKibbin, M., Booth, A., Parry, D., Jain, P., Riazuddin, A., Hejtmancik, J., Khan, S., Firasat, S., Shires, M., Gilmour, D., Towns, K., Murphy, A.-L., Azmanov, D., Tournev, I., Cherninkova, S., Jafri, H., Raashid, Y., Toomes, C., ... Inglehearn, C. (2009). Null mutations in LTBP2 cause primary congenital glaucoma. American Journal of Human Genetics, 84(5), 664-671.

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title = "Null mutations in LTBP2 cause primary congenital glaucoma",

author = "Manir Ali and Martin McKibbin and Adam Booth and David Parry and Payal Jain and Amer Riazuddin and J Hejtmancik and Shaheen Khan and Sabika Firasat and Mike Shires and David Gilmour and Katherine Towns and Anna-Louise Murphy and Dimitar Azmanov and Ivailo Tournev and Sylvia Cherninkova and Hussain Jafri and Yasmin Raashid and C Toomes and Jamie Craig and David Mackey and Luba Kalaydjieva and Sheikh Riazuddin and C Inglehearn",

year = "2009",

language = "English",

volume = "84",

pages = "664--671",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

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Ali, M, McKibbin, M, Booth, A, Parry, D, Jain, P, Riazuddin, A, Hejtmancik, J, Khan, S, Firasat, S, Shires, M, Gilmour, D, Towns, K, Murphy, A-L, Azmanov, D, Tournev, I, Cherninkova, S, Jafri, H, Raashid, Y, Toomes, C, Craig, J, Mackey, D, Kalaydjieva, L, Riazuddin, S & Inglehearn, C 2009, 'Null mutations in LTBP2 cause primary congenital glaucoma', American Journal of Human Genetics, vol. 84, no. 5, pp. 664-671.

TY - JOUR

T1 - Null mutations in LTBP2 cause primary congenital glaucoma

AU - Ali, Manir

AU - McKibbin, Martin

AU - Booth, Adam

AU - Parry, David

AU - Jain, Payal

AU - Riazuddin, Amer

AU - Hejtmancik, J

AU - Khan, Shaheen

AU - Firasat, Sabika

AU - Shires, Mike

AU - Gilmour, David

AU - Towns, Katherine

AU - Murphy, Anna-Louise

AU - Azmanov, Dimitar

AU - Tournev, Ivailo

AU - Cherninkova, Sylvia

AU - Jafri, Hussain

AU - Raashid, Yasmin

AU - Toomes, C

AU - Craig, Jamie

AU - Mackey, David

AU - Kalaydjieva, Luba

AU - Riazuddin, Sheikh

AU - Inglehearn, C

PY - 2009

Y1 - 2009

M3 - Article

SN - 0002-9297

VL - 84

SP - 664

EP - 671

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 5

ER -