First report of molecular diagnosis of Tunisian hemophiliacs A: identification of 8 novel causative mutations.
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Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family.Molecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics Studies.First molecular analysis of F8 gene in algeria: identification of two novel mutations.Molecular diagnosis of haemophilia A in patients from Senegal.
P2860
First report of molecular diagnosis of Tunisian hemophiliacs A: identification of 8 novel causative mutations.
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2012 nî lūn-bûn
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First report of molecular diag ...... f 8 novel causative mutations.
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type
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First report of molecular diag ...... f 8 novel causative mutations.
@en
prefLabel
First report of molecular diag ...... f 8 novel causative mutations.
@en
P2093
P2860
P356
P1433
P1476
First report of molecular diag ...... f 8 novel causative mutations.
@en
P2093
Amel Ben Ammar Elggaaied
Asma Jlizi
Balkis Meddeb
Christine Vinciguerra
Dorothé Pellechia
Edvard Wigren
Emna Gouider
Hejer Elmahmoudi
Houssein Khodjet-el-khil
Kaouther Zahra
P2860
P2888
P356
10.1186/1746-1596-7-93
P577
2012-08-10T00:00:00Z
P5875
P6179
1050963500