A TCTN2 mutation defines a novel Meckel Gruber syndrome...

Human Mutation 2011 Vol. 32; Iss. 6

A TCTN2 mutation defines a novel Meckel Gruber syndrome locus

Ranad Shaheen, Eissa Faqeih, Mohammed Z. Seidahmed, Asma Sunker, Faten Ezzat Alali, AlQahtani Khadijah, Fowzan S. Alkuraya
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Volume:
32
Year:
2011
Language:
english
Pages:
6
DOI:
10.1002/humu.21507
File:
PDF, 298 KB
english, 2011
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