<p>For each family, the phenotype, inheritance model, the altered gene, the identified mutation, the homozygosity/heterozygosity state, and the reference of previously described mutations are indicated. [a] This study, <sup>b</sup>Mutations previously identified by APEX <sup>c</sup>Unknown pathogenicity, <sup>n.i</sup> Not identified.</p
<p>(A) Japanese family of MRX214 with Del 312F in <i>GPR37</i>. (B) Caucasian family of AU0654 with ...
<p>Black symbols indicate clinically affected family members, open symbols indicate unaffected, and ...
<p>CFA = chromosome number; AR = autosomal recessive, XR = X-linked recessive, MP = multifactorial; ...
<p>Missense mutations and the resultant phenotypes observed in the families described in the present...
<p>Below the individuals, genotypes are presented for either p.S1653KfsX2 (M1), p.L2784R (M2), p.Y29...
<p>F, female; Mat, maternal family; Hom/Het, homozygote/heterozygote; SRA, Sequence Read Archive.</p...
<p>Filled symbols represent patients with TRAPS; open squares and circles indicate healthy individua...
<p><b>A:</b> Pedigree and disease-haplotype segregation of family A. Blackened symbols represent aff...
<p>Clinical, pathologic and mutational analysis results for the families that mutations were found i...
<p>Clinical features of three families carrying pathogenic <i>NOTCH1</i> mutations.</p
<p>(a) Family pedigrees are presented in the upper panels. Black symbols denote affected individuals...
<p>The number of carriers and non-carriers in both affected and cognitively normal family members is...
<p>For epidemiological analyses, presented are the number of data points (observations and calculate...
<p>Causative alleles are being listed as “allele 1” and “allele 2” in resolved cases. Additional all...
<p>Summary of five candidate variants with a consistent inheritance pattern detected by whole exome ...
<p>(A) Japanese family of MRX214 with Del 312F in <i>GPR37</i>. (B) Caucasian family of AU0654 with ...
<p>Black symbols indicate clinically affected family members, open symbols indicate unaffected, and ...
<p>CFA = chromosome number; AR = autosomal recessive, XR = X-linked recessive, MP = multifactorial; ...
<p>Missense mutations and the resultant phenotypes observed in the families described in the present...
<p>Below the individuals, genotypes are presented for either p.S1653KfsX2 (M1), p.L2784R (M2), p.Y29...
<p>F, female; Mat, maternal family; Hom/Het, homozygote/heterozygote; SRA, Sequence Read Archive.</p...
<p>Filled symbols represent patients with TRAPS; open squares and circles indicate healthy individua...
<p><b>A:</b> Pedigree and disease-haplotype segregation of family A. Blackened symbols represent aff...
<p>Clinical, pathologic and mutational analysis results for the families that mutations were found i...
<p>Clinical features of three families carrying pathogenic <i>NOTCH1</i> mutations.</p
<p>(a) Family pedigrees are presented in the upper panels. Black symbols denote affected individuals...
<p>The number of carriers and non-carriers in both affected and cognitively normal family members is...
<p>For epidemiological analyses, presented are the number of data points (observations and calculate...
<p>Causative alleles are being listed as “allele 1” and “allele 2” in resolved cases. Additional all...
<p>Summary of five candidate variants with a consistent inheritance pattern detected by whole exome ...
<p>(A) Japanese family of MRX214 with Del 312F in <i>GPR37</i>. (B) Caucasian family of AU0654 with ...
<p>Black symbols indicate clinically affected family members, open symbols indicate unaffected, and ...
<p>CFA = chromosome number; AR = autosomal recessive, XR = X-linked recessive, MP = multifactorial; ...